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nsv6682482

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 27 studies. See in: genome view    
    Submitted genomic127,794,211-127,797,210Question Mark
    Overlapping variant regions from other studies: 139 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):128,551,785-128,554,784Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6682482Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2127,794,211127,797,210
    nsv6682482RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2128,551,785128,554,784

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18441075deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18441075Submitted genomicNC_000002.12:g.127
    794211_127797210de
    l
    GRCh38 (hg38)NC_000002.12Chr2127,794,211127,797,210
    nssv18441075RemappedPerfectNC_000002.11:g.128
    551785_128554784de
    l
    GRCh37.p13First PassNC_000002.11Chr2128,551,785128,554,784

    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)
    nssv184410750.0061595253022
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