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nsv5468478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,953

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 29 studies. See in: genome view    
Submitted genomic40,771,353-40,781,305Question Mark
Overlapping variant regions from other studies: 108 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):40,771,455-40,781,407Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5468478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr540,771,35340,781,305
nsv5468478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr540,771,45540,781,407

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16964494duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16964494Submitted genomicNC_000005.10:g.407
71353_40781305dup
GRCh38 (hg38)NC_000005.10Chr540,771,35340,781,305
nssv16964494RemappedPerfectNC_000005.9:g.4077
1455_40781407dup
GRCh37.p13First PassNC_000005.9Chr540,771,45540,781,407

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)
nssv16964494<0.00116404
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