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nsv6823136

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:255,921

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 922 SVs from 75 studies. See in: genome view    
    Submitted genomic99,031,994-99,287,914Question Mark
    Overlapping variant regions from other studies: 921 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):98,629,617-98,885,537Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6823136Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,031,99499,287,914
    nsv6823136RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr798,629,61798,885,537

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18728726duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18728726Submitted genomicNC_000007.14:g.990
    31994_99287914dup
    GRCh38 (hg38)NC_000007.14Chr799,031,99499,287,914
    nssv18728726RemappedPerfectNC_000007.13:g.986
    29617_98885537dup
    GRCh37.p13First PassNC_000007.13Chr798,629,61798,885,537

    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)
    nssv187287267e-062275762
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