nsv985035

  • Variant Calls:14
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 14 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):36,054,007-36,054,008Question Mark
Overlapping variant regions from other studies: 14 SVs from 7 studies. See in: genome view    
Submitted genomic36,021,784-36,021,785Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv985035RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nsv985035Submitted genomicGRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3374112mobile element insertionTCGA-56-1622SequencingSplit read and paired-end mapping883
nssv3374113mobile element insertionTCGA-60-2698SequencingSplit read and paired-end mapping1,000
nssv3374114mobile element insertionTCGA-CR-6487SequencingSplit read and paired-end mapping1,163
nssv3374115mobile element insertionTCGA-CV-6433SequencingSplit read and paired-end mapping903
nssv3374116mobile element insertionTCGA-CV-7180SequencingSplit read and paired-end mapping1,136
nssv3374117mobile element insertionTCGA-AP-A0LESequencingSplit read and paired-end mapping971
nssv3374118mobile element insertionTCGA-38-4630SequencingSplit read and paired-end mapping726
nssv3374119mobile element insertionTCGA-06-0744SequencingSplit read and paired-end mapping1,155
nssv3374120mobile element insertionTCGA-06-2570SequencingSplit read and paired-end mapping1,113
nssv3374121mobile element insertionTCGA-19-2624SequencingSplit read and paired-end mapping1,059
nssv3374122mobile element insertionTCGA-AB-2978SequencingSplit read and paired-end mapping964
nssv3374123mobile element insertionTCGA-CJ-5682SequencingSplit read and paired-end mapping1,162
nssv3374124mobile element insertionTCGA-24-0982SequencingSplit read and paired-end mapping651
nssv3374125mobile element insertionTCGA-AO-A03NSequencingSplit read and paired-end mapping1,110

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nssv3374112RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374113RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374114RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374115RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374116RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374117RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374118RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374119RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374120RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374121RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374122RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374123RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374124RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374125RemappedPerfectNC_000006.12:g.360
54007_36054008ins(
0_?)
GRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr636,054,00736,054,008
nssv3374112Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374113Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374114Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374115Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374116Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374117Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374118Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374119Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374120Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374121Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374122Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374123Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374124Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785
nssv3374125Submitted genomicNC_000006.11:g.360
21784_36021785ins(
0_?)
GRCh37 (hg19)NC_000006.11Chr636,021,78436,021,785

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant