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nsv6907465

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:656,271

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2276 SVs from 112 studies. See in: genome view    
    Submitted genomic49,565,345-50,221,615Question Mark
    Overlapping variant regions from other studies: 2249 SVs from 112 studies. See in: genome view    
    Remapped(Score: Pass):49,586,897-50,180,786Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6907465Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1149,565,34550,221,615
    nsv6907465RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1149,586,89750,180,786

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350460deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350460Submitted genomicNC_000011.10:g.495
    65345_50221615del
    GRCh38 (hg38)NC_000011.10Chr1149,565,34550,221,615
    nssv18350460RemappedPassNC_000011.9:g.4958
    6897_50180786del
    GRCh37.p13First PassNC_000011.9Chr1149,586,89750,180,786

    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)
    nssv183504604e-061275466
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