U.S. flag

An official website of the United States government

nsv6639846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 200 SVs from 49 studies. See in: genome view    
    Submitted genomic111,285,156-111,293,472Question Mark
    Overlapping variant regions from other studies: 201 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):111,827,778-111,836,094Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6639846Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1111,285,156111,293,472
    nsv6639846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1111,827,778111,836,094

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18346808deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18346808Submitted genomicNC_000001.11:g.111
    285156_111293472de
    l
    GRCh38 (hg38)NC_000001.11Chr1111,285,156111,293,472
    nssv18346808RemappedPerfectNC_000001.10:g.111
    827778_111836094de
    l
    GRCh37.p13First PassNC_000001.10Chr1111,827,778111,836,094

    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)
    nssv18346808<0.001217275822
    Support Center