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nsv6793041

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:513

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 22 studies. See in: genome view    
    Submitted genomic5,004,149-5,004,661Question Mark
    Overlapping variant regions from other studies: 139 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):5,004,383-5,004,895Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793041Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr65,004,1495,004,661
    nsv6793041RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr65,004,3835,004,895

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715939duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715939Submitted genomicNC_000006.12:g.500
    4149_5004661dup
    GRCh38 (hg38)NC_000006.12Chr65,004,1495,004,661
    nssv18715939RemappedPerfectNC_000006.11:g.500
    4383_5004895dup
    GRCh37.p13First PassNC_000006.11Chr65,004,3835,004,895

    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)
    nssv187159394e-061242934
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