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nsv6331876

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,313

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 199 SVs from 49 studies. See in: genome view    
    Submitted genomic111,285,156-111,293,468Question Mark
    Overlapping variant regions from other studies: 200 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):111,827,778-111,836,090Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6331876Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1111,285,156111,293,468
    nsv6331876RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1111,827,778111,836,090

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18050899deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18050899Submitted genomicNC_000001.11:g.111
    285156_111293468de
    l
    GRCh38 (hg38)NC_000001.11Chr1111,285,156111,293,468
    nssv18050899RemappedPerfectNC_000001.10:g.111
    827778_111836090de
    l
    GRCh37.p13First PassNC_000001.10Chr1111,827,778111,836,090

    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)
    nssv18050899<0.001139284
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