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nsv6937745

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 210 SVs from 41 studies. See in: genome view    
    Submitted genomic27,580,601-27,620,200Question Mark
    Overlapping variant regions from other studies: 210 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):28,154,738-28,194,337Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937745Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1327,580,60127,620,200
    nsv6937745RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1328,154,73828,194,337

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600106duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600106Submitted genomicNC_000013.11:g.275
    80601_27620200dup
    GRCh38 (hg38)NC_000013.11Chr1327,580,60127,620,200
    nssv18600106RemappedPerfectNC_000013.10:g.281
    54738_28194337dup
    GRCh37.p13First PassNC_000013.10Chr1328,154,73828,194,337

    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)
    nssv186001064e-061274770
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