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nsv6324901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:460,041

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1486 SVs from 100 studies. See in: genome view    
    Submitted genomic191,625,531-192,085,571Question Mark
    Overlapping variant regions from other studies: 1486 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):191,594,661-192,054,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6324901Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1191,625,531192,085,571
    nsv6324901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1191,594,661192,054,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18055879deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18055879Submitted genomicNC_000001.11:g.191
    625531_192085571de
    l
    GRCh38 (hg38)NC_000001.11Chr1191,625,531192,085,571
    nssv18055879RemappedPerfectNC_000001.10:g.191
    594661_192054701de
    l
    GRCh37.p13First PassNC_000001.10Chr1191,594,661192,054,701

    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)
    nssv18055879<0.001139012
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