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nsv6993008

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 21 studies. See in: genome view    
    Submitted genomic67,432,159-67,432,240Question Mark
    Overlapping variant regions from other studies: 110 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):65,428,275-65,428,356Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993008Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1767,432,15967,432,240
    nsv6993008RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1765,428,27565,428,356

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627517duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627517Submitted genomicNC_000017.11:g.674
    32159_67432240dup
    GRCh38 (hg38)NC_000017.11Chr1767,432,15967,432,240
    nssv18627517RemappedPerfectNC_000017.10:g.654
    28275_65428356dup
    GRCh37.p13First PassNC_000017.10Chr1765,428,27565,428,356

    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)
    nssv186275178.7e-0517191696
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