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nsv7050372

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,979,268

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8963 SVs from 111 studies. See in: genome view    
    Submitted genomic107,280,655-111,259,922Question Mark
    Overlapping variant regions from other studies: 8964 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):107,601,859-111,581,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050372Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6107,280,655111,259,922
    nsv7050372RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6107,601,859111,581,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777804inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777804Submitted genomicNC_000006.12:g.107
    280655_111259922in
    v
    GRCh38 (hg38)NC_000006.12Chr6107,280,655111,259,922
    nssv18777804RemappedPerfectNC_000006.11:g.107
    601859_111581125in
    v
    GRCh37.p13First PassNC_000006.11Chr6107,601,859111,581,125

    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)
    nssv187778044e-061276268
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