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nsv6937927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:118,076

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1123 SVs from 87 studies. See in: genome view    
    Submitted genomic7,720,289-7,838,364Question Mark
    Overlapping variant regions from other studies: 1123 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):7,872,885-7,990,960Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,720,2897,838,364
    nsv6937927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,872,8857,990,960

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18597963duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18597963Submitted genomicNC_000012.12:g.772
    0289_7838364dup
    GRCh38 (hg38)NC_000012.12Chr127,720,2897,838,364
    nssv18597963RemappedPerfectNC_000012.11:g.787
    2885_7990960dup
    GRCh37.p13First PassNC_000012.11Chr127,872,8857,990,960

    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)
    nssv185979634e-061273264
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