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nsv6486406

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,234,175

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7272 SVs from 112 studies. See in: genome view    
    Submitted genomic21,538,051-22,772,225Question Mark
    Overlapping variant regions from other studies: 7460 SVs from 115 studies. See in: genome view    
    Remapped(Score: Good):22,006,185-23,241,434Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6486406Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1421,538,05122,772,225
    nsv6486406RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1422,006,18523,241,434

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18016026deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18016026Submitted genomicNC_000014.9:g.2153
    8051_22772225del
    GRCh38 (hg38)NC_000014.9Chr1421,538,05122,772,225
    nssv18016026RemappedGoodNC_000014.8:g.2200
    6185_23241434del
    GRCh37.p13First PassNC_000014.8Chr1422,006,18523,241,434

    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)
    nssv18016026<0.001137110
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