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nsv7008356

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:518,751

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2186 SVs from 80 studies. See in: genome view    
    Submitted genomic2,884,913-3,403,663Question Mark
    Overlapping variant regions from other studies: 2186 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):2,884,911-3,403,661Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7008356Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr182,884,9133,403,663
    nsv7008356RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr182,884,9113,403,661

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18633399duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18633399Submitted genomicNC_000018.10:g.288
    4913_3403663dup
    GRCh38 (hg38)NC_000018.10Chr182,884,9133,403,663
    nssv18633399RemappedPerfectNC_000018.9:g.2884
    911_3403661dup
    GRCh37.p13First PassNC_000018.9Chr182,884,9113,403,661

    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)
    nssv186333991.4e-054274632
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