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nsv6815161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,887

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 285 SVs from 47 studies. See in: genome view    
    Submitted genomic2,219,594-2,242,480Question Mark
    Overlapping variant regions from other studies: 285 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):2,259,229-2,282,115Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6815161Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,219,5942,242,480
    nsv6815161RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,259,2292,282,115

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18539606deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18539606Submitted genomicNC_000007.14:g.221
    9594_2242480del
    GRCh38 (hg38)NC_000007.14Chr72,219,5942,242,480
    nssv18539606RemappedPerfectNC_000007.13:g.225
    9229_2282115del
    GRCh37.p13First PassNC_000007.13Chr72,259,2292,282,115

    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)
    nssv185396067e-062276234
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