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nsv6475395

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,261,217

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3646 SVs from 109 studies. See in: genome view    
    Submitted genomic104,163,006-105,424,222Question Mark
    Overlapping variant regions from other studies: 3646 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):104,033,734-105,294,949Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6475395Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11104,163,006105,424,222
    nsv6475395RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11104,033,734105,294,949

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18191279duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18191279Submitted genomicNC_000011.10:g.104
    163006_105424222du
    p
    GRCh38 (hg38)NC_000011.10Chr11104,163,006105,424,222
    nssv18191279RemappedPerfectNC_000011.9:g.1040
    33734_105294949dup
    GRCh37.p13First PassNC_000011.9Chr11104,033,734105,294,949

    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)
    nssv18191279<0.001239134
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