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nsv6644985

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:355

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
    Submitted genomic173,865,150-173,865,504Question Mark
    Overlapping variant regions from other studies: 171 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):173,834,288-173,834,642Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644985Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1173,865,150173,865,504
    nsv6644985RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,834,288173,834,642

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582855duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582855Submitted genomicNC_000001.11:g.173
    865150_173865504du
    p
    GRCh38 (hg38)NC_000001.11Chr1173,865,150173,865,504
    nssv18582855RemappedPerfectNC_000001.10:g.173
    834288_173834642du
    p
    GRCh37.p13First PassNC_000001.10Chr1173,834,288173,834,642

    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)
    nssv185828554e-061243544
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