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nsv7081963

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:150,612

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 430 SVs from 49 studies. See in: genome view    
    Submitted genomic96,827,069-96,977,680Question Mark
    Overlapping variant regions from other studies: 430 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):96,082,068-96,232,679Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7081963Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX96,827,06996,977,680
    nsv7081963RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX96,082,06896,232,679

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18660481duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18660481Submitted genomicNC_000023.11:g.968
    27069_96977680dup
    GRCh38 (hg38)NC_000023.11ChrX96,827,06996,977,680
    nssv18660481RemappedPerfectNC_000023.10:g.960
    82068_96232679dup
    GRCh37.p13First PassNC_000023.10ChrX96,082,06896,232,679

    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)
    nssv186604815e-061200000
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