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nsv6975681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:212,434

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 584 SVs from 65 studies. See in: genome view    
    Submitted genomic70,562,447-70,774,880Question Mark
    Overlapping variant regions from other studies: 584 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):71,029,164-71,241,597Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1470,562,44770,774,880
    nsv6975681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1471,029,16471,241,597

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612745duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612745Submitted genomicNC_000014.9:g.7056
    2447_70774880dup
    GRCh38 (hg38)NC_000014.9Chr1470,562,44770,774,880
    nssv18612745RemappedPerfectNC_000014.8:g.7102
    9164_71241597dup
    GRCh37.p13First PassNC_000014.8Chr1471,029,16471,241,597

    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)
    nssv186127454e-061276016
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