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nsv6765448

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,977

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
    Submitted genomic93,734,997-93,742,973Question Mark
    Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):93,070,703-93,078,679Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6765448Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr593,734,99793,742,973
    nsv6765448RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr593,070,70393,078,679

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18707654duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18707654Submitted genomicNC_000005.10:g.937
    34997_93742973dup
    GRCh38 (hg38)NC_000005.10Chr593,734,99793,742,973
    nssv18707654RemappedPerfectNC_000005.9:g.9307
    0703_93078679dup
    GRCh37.p13First PassNC_000005.9Chr593,070,70393,078,679

    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)
    nssv187076544e-061274808
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