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nsv6472998

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,292

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 69 SVs from 17 studies. See in: genome view    
    Submitted genomic60,943,394-60,946,685Question Mark
    Overlapping variant regions from other studies: 69 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):60,710,866-60,714,157Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6472998Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1160,943,39460,946,685
    nsv6472998RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1160,710,86660,714,157

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992670deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992670Submitted genomicNC_000011.10:g.609
    43394_60946685del
    GRCh38 (hg38)NC_000011.10Chr1160,943,39460,946,685
    nssv17992670RemappedPerfectNC_000011.9:g.6071
    0866_60714157del
    GRCh37.p13First PassNC_000011.9Chr1160,710,86660,714,157

    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)
    nssv17992670<0.001138992
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