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nsv6858499

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
    Submitted genomic94,242,310-94,242,709Question Mark
    Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):97,004,592-97,004,991Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6858499Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr994,242,31094,242,709
    nsv6858499RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr997,004,59297,004,991

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749075duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749075Submitted genomicNC_000009.12:g.942
    42310_94242709dup
    GRCh38 (hg38)NC_000009.12Chr994,242,31094,242,709
    nssv18749075RemappedPerfectNC_000009.11:g.970
    04592_97004991dup
    GRCh37.p13First PassNC_000009.11Chr997,004,59297,004,991

    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)
    nssv18749075<0.001126234866
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