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nsv6986991

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:604,393

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1685 SVs from 77 studies. See in: genome view    
    Submitted genomic57,059,649-57,664,041Question Mark
    Overlapping variant regions from other studies: 1685 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):57,093,561-57,697,953Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986991Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1657,059,64957,664,041
    nsv6986991RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1657,093,56157,697,953

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18621606duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18621606Submitted genomicNC_000016.10:g.570
    59649_57664041dup
    GRCh38 (hg38)NC_000016.10Chr1657,059,64957,664,041
    nssv18621606RemappedPerfectNC_000016.9:g.5709
    3561_57697953dup
    GRCh37.p13First PassNC_000016.9Chr1657,093,56157,697,953

    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)
    nssv186216064e-061275788
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