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nsv6731144

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:758,536

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1560 SVs from 83 studies. See in: genome view    
    Submitted genomic158,442,060-159,200,595Question Mark
    Overlapping variant regions from other studies: 1560 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):158,159,849-158,918,384Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6731144Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3158,442,060159,200,595
    nsv6731144RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3158,159,849158,918,384

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18673702duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18673702Submitted genomicNC_000003.12:g.158
    442060_159200595du
    p
    GRCh38 (hg38)NC_000003.12Chr3158,442,060159,200,595
    nssv18673702RemappedPerfectNC_000003.11:g.158
    159849_158918384du
    p
    GRCh37.p13First PassNC_000003.11Chr3158,159,849158,918,384

    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)
    nssv186737024e-061270700
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