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nsv6793309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,427

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 348 SVs from 53 studies. See in: genome view    
    Submitted genomic34,382,387-34,439,813Question Mark
    Overlapping variant regions from other studies: 348 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):34,350,164-34,407,590Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr634,382,38734,439,813
    nsv6793309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr634,350,16434,407,590

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18712831duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18712831Submitted genomicNC_000006.12:g.343
    82387_34439813dup
    GRCh38 (hg38)NC_000006.12Chr634,382,38734,439,813
    nssv18712831RemappedPerfectNC_000006.11:g.343
    50164_34407590dup
    GRCh37.p13First PassNC_000006.11Chr634,350,16434,407,590

    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)
    nssv187128314e-061265882
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