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nsv7053014

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:475,666

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1173 SVs from 75 studies. See in: genome view    
    Submitted genomic107,397,622-107,873,287Question Mark
    Overlapping variant regions from other studies: 1173 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):107,718,826-108,194,491Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053014Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6107,397,622107,873,287
    nsv7053014RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6107,718,826108,194,491

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777807inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777807Submitted genomicNC_000006.12:g.107
    397622_107873287in
    v
    GRCh38 (hg38)NC_000006.12Chr6107,397,622107,873,287
    nssv18777807RemappedPerfectNC_000006.11:g.107
    718826_108194491in
    v
    GRCh37.p13First PassNC_000006.11Chr6107,718,826108,194,491

    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)
    nssv187778077e-062275182
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