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nsv6344721

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:622

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
    Submitted genomic216,691,841-216,692,462Question Mark
    Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):217,556,564-217,557,185Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6344721Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2216,691,841216,692,462
    nsv6344721RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2217,556,564217,557,185

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205621duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205621Submitted genomicNC_000002.12:g.216
    691841_216692462du
    p
    GRCh38 (hg38)NC_000002.12Chr2216,691,841216,692,462
    nssv18205621RemappedPerfectNC_000002.11:g.217
    556564_217557185du
    p
    GRCh37.p13First PassNC_000002.11Chr2217,556,564217,557,185

    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)
    nssv18205621<0.001437340
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