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nsv6467543

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,178

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 55 SVs from 15 studies. See in: genome view    
    Submitted genomic59,591,810-59,592,987Question Mark
    Overlapping variant regions from other studies: 55 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):59,359,283-59,360,460Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6467543Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1159,591,81059,592,987
    nsv6467543RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1159,359,28359,360,460

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992460deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992460Submitted genomicNC_000011.10:g.595
    91810_59592987del
    GRCh38 (hg38)NC_000011.10Chr1159,591,81059,592,987
    nssv17992460RemappedPerfectNC_000011.9:g.5935
    9283_59360460del
    GRCh37.p13First PassNC_000011.9Chr1159,359,28359,360,460

    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)
    nssv17992460<0.001137690
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