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nsv6906649

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,863

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 192 SVs from 42 studies. See in: genome view    
    Submitted genomic93,300,343-93,336,205Question Mark
    Overlapping variant regions from other studies: 192 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):93,033,509-93,069,371Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6906649Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1193,300,34393,336,205
    nsv6906649RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1193,033,50993,069,371

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18355045deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18355045Submitted genomicNC_000011.10:g.933
    00343_93336205del
    GRCh38 (hg38)NC_000011.10Chr1193,300,34393,336,205
    nssv18355045RemappedPerfectNC_000011.9:g.9303
    3509_93069371del
    GRCh37.p13First PassNC_000011.9Chr1193,033,50993,069,371

    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)
    nssv183550454e-061276196
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