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nsv6345022

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:711,094

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1395 SVs from 72 studies. See in: genome view    
    Submitted genomic206,375,924-207,087,017Question Mark
    Overlapping variant regions from other studies: 1395 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):207,240,648-207,951,741Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6345022Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2206,375,924207,087,017
    nsv6345022RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2207,240,648207,951,741

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18208099duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18208099Submitted genomicNC_000002.12:g.206
    375924_207087017du
    p
    GRCh38 (hg38)NC_000002.12Chr2206,375,924207,087,017
    nssv18208099RemappedPerfectNC_000002.11:g.207
    240648_207951741du
    p
    GRCh37.p13First PassNC_000002.11Chr2207,240,648207,951,741

    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)
    nssv18208099<0.001139258
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