nsv441684

  • Variant Calls:4
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,201

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 395 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):16,041,636-16,052,836Question Mark
Overlapping variant regions from other studies: 395 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):16,368,131-16,379,331Question Mark
Overlapping variant regions from other studies: 29 SVs from 8 studies. See in: genome view    
Submitted genomic16,113,437-16,124,637Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv441684RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,041,63616,052,836
nsv441684RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,368,13116,379,331
nsv441684Submitted genomicNCBI35 (hg17)NC_000001.8Chr116,113,43716,124,637

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv1656596copy number gainNA10846SNP arrayProbe signal intensity3156
nssv1656597copy number gainNA12144SNP arrayProbe signal intensity3151
nssv1656598copy number gainNA18508SNP arrayProbe signal intensity3192
nssv1656599copy number gainNA19159SNP arrayProbe signal intensity3195

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1656596RemappedPerfectNC_000001.11:g.(?_
16041636)_(1605283
6_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,041,63616,052,836
nssv1656597RemappedPerfectNC_000001.11:g.(?_
16041636)_(1605283
6_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,041,63616,052,836
nssv1656598RemappedPerfectNC_000001.11:g.(?_
16041636)_(1605283
6_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,041,63616,052,836
nssv1656599RemappedPerfectNC_000001.11:g.(?_
16041636)_(1605283
6_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr116,041,63616,052,836
nssv1656596RemappedPerfectNC_000001.10:g.(?_
16368131)_(1637933
1_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,368,13116,379,331
nssv1656597RemappedPerfectNC_000001.10:g.(?_
16368131)_(1637933
1_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,368,13116,379,331
nssv1656598RemappedPerfectNC_000001.10:g.(?_
16368131)_(1637933
1_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,368,13116,379,331
nssv1656599RemappedPerfectNC_000001.10:g.(?_
16368131)_(1637933
1_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr116,368,13116,379,331
nssv1656596Submitted genomicNC_000001.8:g.(?_1
6113437)_(16124637
_?)dup
NCBI35 (hg17)NC_000001.8Chr116,113,43716,124,637
nssv1656597Submitted genomicNC_000001.8:g.(?_1
6113437)_(16124637
_?)dup
NCBI35 (hg17)NC_000001.8Chr116,113,43716,124,637
nssv1656598Submitted genomicNC_000001.8:g.(?_1
6113437)_(16124637
_?)dup
NCBI35 (hg17)NC_000001.8Chr116,113,43716,124,637
nssv1656599Submitted genomicNC_000001.8:g.(?_1
6113437)_(16124637
_?)dup
NCBI35 (hg17)NC_000001.8Chr116,113,43716,124,637

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

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