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nsv6785753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:670,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1956 SVs from 83 studies. See in: genome view    
    Submitted genomic42,646,801-43,317,300Question Mark
    Overlapping variant regions from other studies: 1956 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):42,614,539-43,285,038Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr642,646,80143,317,300
    nsv6785753RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr642,614,53943,285,038

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715530duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715530Submitted genomicNC_000006.12:g.426
    46801_43317300dup
    GRCh38 (hg38)NC_000006.12Chr642,646,80143,317,300
    nssv18715530RemappedPerfectNC_000006.11:g.426
    14539_43285038dup
    GRCh37.p13First PassNC_000006.11Chr642,614,53943,285,038

    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)
    nssv18715530<0.00145268758
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