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nsv6419361

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:811

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 24 studies. See in: genome view    
    Submitted genomic66,637,708-66,638,518Question Mark
    Overlapping variant regions from other studies: 132 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):67,549,943-67,550,753Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6419361Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr866,637,70866,638,518
    nsv6419361RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr867,549,94367,550,753

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18169417deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18169417Submitted genomicNC_000008.11:g.666
    37708_66638518del
    GRCh38 (hg38)NC_000008.11Chr866,637,70866,638,518
    nssv18169417RemappedPerfectNC_000008.10:g.675
    49943_67550753del
    GRCh37.p13First PassNC_000008.10Chr867,549,94367,550,753

    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)
    nssv18169417<0.001636434
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