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nsv6786283

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:758

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
    Submitted genomic26,158,289-26,159,046Question Mark
    Overlapping variant regions from other studies: 144 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):26,158,517-26,159,274Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6786283Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,158,28926,159,046
    nsv6786283RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,158,51726,159,274

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18524957deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18524957Submitted genomicNC_000006.12:g.261
    58289_26159046del
    GRCh38 (hg38)NC_000006.12Chr626,158,28926,159,046
    nssv18524957RemappedPerfectNC_000006.11:g.261
    58517_26159274del
    GRCh37.p13First PassNC_000006.11Chr626,158,51726,159,274

    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)
    nssv185249574e-061275028
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