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nsv5492967

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,026

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 27 studies. See in: genome view    
Submitted genomic95,896,689-95,909,714Question Mark
Overlapping variant regions from other studies: 119 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):95,526,001-95,539,026Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492967Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr795,896,68995,909,714
nsv5492967RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr795,526,00195,539,026

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17002181deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17002181Submitted genomicNC_000007.14:g.958
96689_95909714del
GRCh38 (hg38)NC_000007.14Chr795,896,68995,909,714
nssv17002181RemappedPerfectNC_000007.13:g.955
26001_95539026del
GRCh37.p13First PassNC_000007.13Chr795,526,00195,539,026

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)
nssv17002181<0.00116404
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