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nsv6948290

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,859

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
    Submitted genomic20,735,383-20,747,241Question Mark
    Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):21,203,542-21,215,400Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6948290Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1420,735,38320,747,241
    nsv6948290RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1421,203,54221,215,400

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18383891deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18383891Submitted genomicNC_000014.9:g.2073
    5383_20747241del
    GRCh38 (hg38)NC_000014.9Chr1420,735,38320,747,241
    nssv18383891RemappedPerfectNC_000014.8:g.2120
    3542_21215400del
    GRCh37.p13First PassNC_000014.8Chr1421,203,54221,215,400

    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)
    nssv183838914e-061276258
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