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nsv6473210

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,373

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 25 studies. See in: genome view    
    Submitted genomic74,198,076-74,201,448Question Mark
    Overlapping variant regions from other studies: 91 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):73,909,121-73,912,493Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6473210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,198,07674,201,448
    nsv6473210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,909,12173,912,493

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17993904deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17993904Submitted genomicNC_000011.10:g.741
    98076_74201448del
    GRCh38 (hg38)NC_000011.10Chr1174,198,07674,201,448
    nssv17993904RemappedPerfectNC_000011.9:g.7390
    9121_73912493del
    GRCh37.p13First PassNC_000011.9Chr1173,909,12173,912,493

    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)
    nssv17993904<0.001139204
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