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nsv4600682

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:509

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):122,990,274-122,990,782Question Mark
    Overlapping variant regions from other studies: 147 SVs from 21 studies. See in: genome view    
    Submitted genomic124,749,790-124,750,298Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4600682RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10122,990,274122,990,782
    nsv4600682Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr10124,749,790124,750,298

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16114173duplicationCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16114173RemappedPerfectNC_000010.11:g.(?_
    122990274)_(122990
    782_?)dup
    GRCh38.p12First PassNC_000010.11Chr10122,990,274122,990,782
    nssv16114173Submitted genomicNC_000010.10:g.(?_
    124749790)_(124750
    298_?)dup
    GRCh37 (hg19)NC_000010.10Chr10124,749,790124,750,298

    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)
    nssv161141730.0011845
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