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nsv6330053

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,686

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 25 studies. See in: genome view    
    Submitted genomic116,961,955-116,965,640Question Mark
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):117,504,577-117,508,262Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330053Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1116,961,955116,965,640
    nsv6330053RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1117,504,577117,508,262

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18051828deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18051828Submitted genomicNC_000001.11:g.116
    961955_116965640de
    l
    GRCh38 (hg38)NC_000001.11Chr1116,961,955116,965,640
    nssv18051828RemappedPerfectNC_000001.10:g.117
    504577_117508262de
    l
    GRCh37.p13First PassNC_000001.10Chr1117,504,577117,508,262

    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)
    nssv18051828<0.001239256
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