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nsv6322462

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:416

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 28 studies. See in: genome view    
    Submitted genomic51,138,908-51,139,323Question Mark
    Overlapping variant regions from other studies: 129 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):51,604,580-51,604,995Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6322462Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr151,138,90851,139,323
    nsv6322462RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr151,604,58051,604,995

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18061965deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18061965Submitted genomicNC_000001.11:g.511
    38908_51139323del
    GRCh38 (hg38)NC_000001.11Chr151,138,90851,139,323
    nssv18061965RemappedPerfectNC_000001.10:g.516
    04580_51604995del
    GRCh37.p13First PassNC_000001.10Chr151,604,58051,604,995

    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)
    nssv18061965<0.001134866
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