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nsv6926735

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 247 SVs from 53 studies. See in: genome view    
    Submitted genomic27,604,501-27,613,000Question Mark
    Overlapping variant regions from other studies: 247 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):27,757,434-27,765,933Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6926735Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1227,604,50127,613,000
    nsv6926735RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1227,757,43427,765,933

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18596661duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18596661Submitted genomicNC_000012.12:g.276
    04501_27613000dup
    GRCh38 (hg38)NC_000012.12Chr1227,604,50127,613,000
    nssv18596661RemappedPerfectNC_000012.11:g.277
    57434_27765933dup
    GRCh37.p13First PassNC_000012.11Chr1227,757,43427,765,933

    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)
    nssv185966616.8e-0519275432
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