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nsv6680732

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121,531

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 389 SVs from 38 studies. See in: genome view    
    Submitted genomic165,784,282-165,905,812Question Mark
    Overlapping variant regions from other studies: 389 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):166,640,792-166,762,322Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6680732Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2165,784,282165,905,812
    nsv6680732RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2166,640,792166,762,322

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18649877duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18649877Submitted genomicNC_000002.12:g.165
    784282_165905812du
    p
    GRCh38 (hg38)NC_000002.12Chr2165,784,282165,905,812
    nssv18649877RemappedPerfectNC_000002.11:g.166
    640792_166762322du
    p
    GRCh37.p13First PassNC_000002.11Chr2166,640,792166,762,322

    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)
    nssv186498771.8e-055272938
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