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nsv6691337

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,258

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
    Submitted genomic149,016,827-149,020,084Question Mark
    Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):149,873,341-149,876,598Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6691337Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2149,016,827149,020,084
    nsv6691337RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2149,873,341149,876,598

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18444116deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18444116Submitted genomicNC_000002.12:g.149
    016827_149020084de
    l
    GRCh38 (hg38)NC_000002.12Chr2149,016,827149,020,084
    nssv18444116RemappedPerfectNC_000002.11:g.149
    873341_149876598de
    l
    GRCh37.p13First PassNC_000002.11Chr2149,873,341149,876,598

    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)
    nssv18444116<0.00123275638
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