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nsv6952699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
    Submitted genomic74,385,452-74,385,585Question Mark
    Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):74,959,589-74,959,722Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6952699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1374,385,45274,385,585
    nsv6952699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1374,959,58974,959,722

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18605960duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18605960Submitted genomicNC_000013.11:g.743
    85452_74385585dup
    GRCh38 (hg38)NC_000013.11Chr1374,385,45274,385,585
    nssv18605960RemappedPerfectNC_000013.10:g.749
    59589_74959722dup
    GRCh37.p13First PassNC_000013.10Chr1374,959,58974,959,722

    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)
    nssv186059608.2e-0519226422
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