nsv441682

  • Variant Calls:4
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,102

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):15,162,689-15,163,790Question Mark
Overlapping variant regions from other studies: 97 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):15,489,185-15,490,286Question Mark
Overlapping variant regions from other studies: 6 SVs from 4 studies. See in: genome view    
Submitted genomic15,234,491-15,235,592Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv441682RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr115,162,68915,163,790
nsv441682RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr115,489,18515,490,286
nsv441682Submitted genomicNCBI35 (hg17)NC_000001.8Chr115,234,49115,235,592

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv1656588copy number lossNA19102SNP arrayProbe signal intensity1173
nssv1656589copy number lossNA19103SNP arrayProbe signal intensity1172
nssv1656590copy number lossNA19206SNP arrayProbe signal intensity0185
nssv1656591copy number lossNA19208SNP arrayProbe signal intensity1155

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1656588RemappedPerfectNC_000001.11:g.(?_
15162689)_(1516379
0_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr115,162,68915,163,790
nssv1656589RemappedPerfectNC_000001.11:g.(?_
15162689)_(1516379
0_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr115,162,68915,163,790
nssv1656590RemappedPerfectNC_000001.11:g.(?_
15162689)_(1516379
0_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr115,162,68915,163,790
nssv1656591RemappedPerfectNC_000001.11:g.(?_
15162689)_(1516379
0_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr115,162,68915,163,790
nssv1656588RemappedPerfectNC_000001.10:g.(?_
15489185)_(1549028
6_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr115,489,18515,490,286
nssv1656589RemappedPerfectNC_000001.10:g.(?_
15489185)_(1549028
6_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr115,489,18515,490,286
nssv1656590RemappedPerfectNC_000001.10:g.(?_
15489185)_(1549028
6_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr115,489,18515,490,286
nssv1656591RemappedPerfectNC_000001.10:g.(?_
15489185)_(1549028
6_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr115,489,18515,490,286
nssv1656588Submitted genomicNC_000001.8:g.(?_1
5234491)_(15235592
_?)del
NCBI35 (hg17)NC_000001.8Chr115,234,49115,235,592
nssv1656589Submitted genomicNC_000001.8:g.(?_1
5234491)_(15235592
_?)del
NCBI35 (hg17)NC_000001.8Chr115,234,49115,235,592
nssv1656590Submitted genomicNC_000001.8:g.(?_1
5234491)_(15235592
_?)del
NCBI35 (hg17)NC_000001.8Chr115,234,49115,235,592
nssv1656591Submitted genomicNC_000001.8:g.(?_1
5234491)_(15235592
_?)del
NCBI35 (hg17)NC_000001.8Chr115,234,49115,235,592

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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