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nsv6345829

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:766,817

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2330 SVs from 95 studies. See in: genome view    
    Submitted genomic193,282,403-194,049,219Question Mark
    Overlapping variant regions from other studies: 2330 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):194,147,128-194,913,943Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6345829Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2193,282,403194,049,219
    nsv6345829RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2194,147,128194,913,943

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205464duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205464Submitted genomicNC_000002.12:g.193
    282403_194049219du
    p
    GRCh38 (hg38)NC_000002.12Chr2193,282,403194,049,219
    nssv18205464RemappedPerfectNC_000002.11:g.194
    147128_194913943du
    p
    GRCh37.p13First PassNC_000002.11Chr2194,147,128194,913,943

    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)
    nssv18205464<0.001138482
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