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nsv6848111

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:267,918

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1128 SVs from 70 studies. See in: genome view    
    Submitted genomic129,844,538-130,112,455Question Mark
    Overlapping variant regions from other studies: 1128 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):130,856,784-131,124,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6848111Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8129,844,538130,112,455
    nsv6848111RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8130,856,784131,124,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734563duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734563Submitted genomicNC_000008.11:g.129
    844538_130112455du
    p
    GRCh38 (hg38)NC_000008.11Chr8129,844,538130,112,455
    nssv18734563RemappedPerfectNC_000008.10:g.130
    856784_131124701du
    p
    GRCh37.p13First PassNC_000008.10Chr8130,856,784131,124,701

    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)
    nssv187345639.6e-0527275084
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