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nsv6910311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189,293

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 486 SVs from 63 studies. See in: genome view    
    Submitted genomic71,721,399-71,910,691Question Mark
    Overlapping variant regions from other studies: 486 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):71,432,445-71,621,737Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6910311Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1171,721,39971,910,691
    nsv6910311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1171,432,44571,621,737

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352307deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352307Submitted genomicNC_000011.10:g.717
    21399_71910691del
    GRCh38 (hg38)NC_000011.10Chr1171,721,39971,910,691
    nssv18352307RemappedPerfectNC_000011.9:g.7143
    2445_71621737del
    GRCh37.p13First PassNC_000011.9Chr1171,432,44571,621,737

    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)
    nssv183523074e-061275268
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