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nsv6464655

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,901

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 202 SVs from 41 studies. See in: genome view    
    Submitted genomic124,214,879-124,224,779Question Mark
    Overlapping variant regions from other studies: 203 SVs from 41 studies. See in: genome view    
    Remapped(Score: Good):124,085,586-124,095,484Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6464655Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,214,879124,224,779
    nsv6464655RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,085,586124,095,484

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17987795deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17987795Submitted genomicNC_000011.10:g.124
    214879_124224779de
    l
    GRCh38 (hg38)NC_000011.10Chr11124,214,879124,224,779
    nssv17987795RemappedGoodNC_000011.9:g.1240
    85586_124095484del
    GRCh37.p13First PassNC_000011.9Chr11124,085,586124,095,484

    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)
    nssv17987795<0.001139220
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