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nsv6960558

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,529

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 361 SVs from 41 studies. See in: genome view    
    Submitted genomic2,151,269-2,158,797Question Mark
    Overlapping variant regions from other studies: 361 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):2,201,270-2,208,798Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960558Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr162,151,2692,158,797
    nsv6960558RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr162,201,2702,208,798

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18399380deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18399380Submitted genomicNC_000016.10:g.215
    1269_2158797del
    GRCh38 (hg38)NC_000016.10Chr162,151,2692,158,797
    nssv18399380RemappedPerfectNC_000016.9:g.2201
    270_2208798del
    GRCh37.p13First PassNC_000016.9Chr162,201,2702,208,798

    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)
    nssv183993804e-061276178
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