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nsv7036183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 26 studies. See in: genome view    
    Submitted genomic42,741,765-42,741,845Question Mark
    Overlapping variant regions from other studies: 187 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):44,161,875-44,161,955Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7036183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2142,741,76542,741,845
    nsv7036183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2144,161,87544,161,955

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644098duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644098Submitted genomicNC_000021.9:g.4274
    1765_42741845dup
    GRCh38 (hg38)NC_000021.9Chr2142,741,76542,741,845
    nssv18644098RemappedPerfectNC_000021.8:g.4416
    1875_44161955dup
    GRCh37.p13First PassNC_000021.8Chr2144,161,87544,161,955

    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)
    nssv186440987.4e-056213116
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