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nsv5475163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:373,659

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1963 SVs from 108 studies. See in: genome view    
Submitted genomic76,693,432-77,067,090Question Mark
Overlapping variant regions from other studies: 1960 SVs from 109 studies. See in: genome view    
Remapped(Score: Perfect):76,322,749-76,696,407Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr776,693,43277,067,090
nsv5475163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr776,322,74976,696,407

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001134duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001134Submitted genomicNC_000007.14:g.766
93432_77067090dup
GRCh38 (hg38)NC_000007.14Chr776,693,43277,067,090
nssv17001134RemappedPerfectNC_000007.13:g.763
22749_76696407dup
GRCh37.p13First PassNC_000007.13Chr776,322,74976,696,407

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)
nssv170011340.021256402
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