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nsv6475350

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,931,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7511 SVs from 112 studies. See in: genome view    
    Submitted genomic104,112,101-107,043,900Question Mark
    Overlapping variant regions from other studies: 7513 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):103,982,829-106,914,626Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6475350Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11104,112,101107,043,900
    nsv6475350RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11103,982,829106,914,626

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17986056deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17986056Submitted genomicNC_000011.10:g.104
    112101_107043900de
    l
    GRCh38 (hg38)NC_000011.10Chr11104,112,101107,043,900
    nssv17986056RemappedPerfectNC_000011.9:g.1039
    82829_106914626del
    GRCh37.p13First PassNC_000011.9Chr11103,982,829106,914,626

    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)
    nssv17986056<0.001138942
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