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nsv4604087

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:740,899

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3122 SVs from 101 studies. See in: genome view    
    Remapped(Score: Good):57,063,207-57,804,105Question Mark
    Overlapping variant regions from other studies: 3169 SVs from 102 studies. See in: genome view    
    Submitted genomic57,130,914-57,863,811Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4604087RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr757,063,20757,804,105
    nsv4604087Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr757,130,91457,863,811

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16123421duplicationCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16123421RemappedGoodNC_000007.14:g.(?_
    57063207)_(5780410
    5_?)dup
    GRCh38.p12First PassNC_000007.14Chr757,063,20757,804,105
    nssv16123421Submitted genomicNC_000007.13:g.(?_
    57130914)_(5786381
    1_?)dup
    GRCh37 (hg19)NC_000007.13Chr757,130,91457,863,811

    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)
    nssv16123421<0.00145919
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