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nsv5477961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:751

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 176 SVs from 21 studies. See in: genome view    
Submitted genomic155,642,651-155,643,401Question Mark
Overlapping variant regions from other studies: 176 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):155,435,345-155,436,095Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5477961Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7155,642,651155,643,401
nsv5477961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7155,435,345155,436,095

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17005931deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17005931Submitted genomicNC_000007.14:g.155
642651_155643401de
l
GRCh38 (hg38)NC_000007.14Chr7155,642,651155,643,401
nssv17005931RemappedPerfectNC_000007.13:g.155
435345_155436095de
l
GRCh37.p13First PassNC_000007.13Chr7155,435,345155,436,095

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17005931<0.00126404
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