nsv821609

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:199,215

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1299 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):144,178,555-144,377,769Question Mark
Overlapping variant regions from other studies: 1299 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):143,875,648-144,074,862Question Mark
Overlapping variant regions from other studies: 1123 SVs from 30 studies. See in: genome view    
Submitted genomic143,506,581-143,705,795Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821609RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000007.14Chr7144,178,555144,377,769
nsv821609RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000007.13Chr7143,875,648144,074,862
nsv821609Submitted genomicNCBI36 (hg18)NC_000007.12Chr7143,506,581143,705,795

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1420704duplicationNA10851SequencingRead depth1,299

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1420704RemappedPerfectNC_000007.14:g.(?_
144178555)_(144377
769_?)dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000007.14Chr7144,178,555144,377,769
nssv1420704RemappedPerfectNC_000007.13:g.(?_
143875648)_(144074
862_?)dup
GRCh37 (hg19)Primary AssemblyFirst PassNC_000007.13Chr7143,875,648144,074,862
nssv1420704Submitted genomicNC_000007.12:g.(?_
143506581)_(143705
795_?)dup
NCBI36 (hg18)NC_000007.12Chr7143,506,581143,705,795

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

Support Center