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nsv4617989

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:764,532

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1504 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):112,357,594-113,122,125Question Mark
    Overlapping variant regions from other studies: 1505 SVs from 74 studies. See in: genome view    
    Submitted genomic112,228,317-112,992,847Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4617989RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11112,357,594113,122,125
    nsv4617989Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr11112,228,317112,992,847

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16126004duplicationCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16126004RemappedPerfectNC_000011.10:g.(?_
    112357594)_(113122
    125_?)dup
    GRCh38.p12First PassNC_000011.10Chr11112,357,594113,122,125
    nssv16126004Submitted genomicNC_000011.9:g.(?_1
    12228317)_(1129928
    47_?)dup
    GRCh37 (hg19)NC_000011.9Chr11112,228,317112,992,847

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv16126004<0.00115919
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