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nsv6984815

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,185

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 320 SVs from 56 studies. See in: genome view    
    Submitted genomic74,582,269-74,615,453Question Mark
    Overlapping variant regions from other studies: 320 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):72,578,408-72,611,592Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6984815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1774,582,26974,615,453
    nsv6984815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1772,578,40872,611,592

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631228duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631228Submitted genomicNC_000017.11:g.745
    82269_74615453dup
    GRCh38 (hg38)NC_000017.11Chr1774,582,26974,615,453
    nssv18631228RemappedPerfectNC_000017.10:g.725
    78408_72611592dup
    GRCh37.p13First PassNC_000017.10Chr1772,578,40872,611,592

    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)
    nssv186312284e-061275682
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