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nsv6968854

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:136,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 705 SVs from 55 studies. See in: genome view    
    Submitted genomic50,629,601-50,765,600Question Mark
    Overlapping variant regions from other studies: 705 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):50,921,798-51,057,797Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968854Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1550,629,60150,765,600
    nsv6968854RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1550,921,79851,057,797

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615819duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615819Submitted genomicNC_000015.10:g.506
    29601_50765600dup
    GRCh38 (hg38)NC_000015.10Chr1550,629,60150,765,600
    nssv18615819RemappedPerfectNC_000015.9:g.5092
    1798_51057797dup
    GRCh37.p13First PassNC_000015.9Chr1550,921,79851,057,797

    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)
    nssv18615819<0.00157240118
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