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nsv4591976

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):13,574,607-13,574,740Question Mark
    Overlapping variant regions from other studies: 126 SVs from 21 studies. See in: genome view    
    Submitted genomic13,574,839-13,574,972Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4591976RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr613,574,60713,574,740
    nsv4591976Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr613,574,83913,574,972

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16123535duplicationCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16123535RemappedPerfectNC_000006.12:g.(?_
    13574607)_(1357474
    0_?)dup
    GRCh38.p12First PassNC_000006.12Chr613,574,60713,574,740
    nssv16123535Submitted genomicNC_000006.11:g.(?_
    13574839)_(1357497
    2_?)dup
    GRCh37 (hg19)NC_000006.11Chr613,574,83913,574,972

    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)
    nssv161235350.0065845
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