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nsv6912322

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,114

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 36 studies. See in: genome view    
    Submitted genomic3,405,578-3,407,691Question Mark
    Overlapping variant regions from other studies: 116 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):3,426,808-3,428,921Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912322Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr113,405,5783,407,691
    nsv6912322RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr113,426,8083,428,921

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18349093deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18349093Submitted genomicNC_000011.10:g.340
    5578_3407691del
    GRCh38 (hg38)NC_000011.10Chr113,405,5783,407,691
    nssv18349093RemappedPerfectNC_000011.9:g.3426
    808_3428921del
    GRCh37.p13First PassNC_000011.9Chr113,426,8083,428,921

    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)
    nssv183490934e-061270404
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