nsv6656540

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 39 studies. See in: genome view    
    Submitted genomic86,631,201-86,637,100Question Mark
    Overlapping variant regions from other studies: 179 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):87,096,884-87,102,783Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6656540Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr186,631,20186,637,100
    nsv6656540RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr187,096,88487,102,783

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18427664deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18427664Submitted genomicNC_000001.11:g.866
    31201_86637100del
    GRCh38 (hg38)NC_000001.11Chr186,631,20186,637,100
    nssv18427664RemappedPerfectNC_000001.10:g.870
    96884_87102783del
    GRCh37.p13First PassNC_000001.10Chr187,096,88487,102,783

    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)
    nssv184276649.9e-0526258204
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