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nsv6967230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134,596

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 516 SVs from 57 studies. See in: genome view    
    Submitted genomic40,677,546-40,812,141Question Mark
    Overlapping variant regions from other studies: 516 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):40,969,744-41,104,339Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6967230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,677,54640,812,141
    nsv6967230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1540,969,74441,104,339

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18618727duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18618727Submitted genomicNC_000015.10:g.406
    77546_40812141dup
    GRCh38 (hg38)NC_000015.10Chr1540,677,54640,812,141
    nssv18618727RemappedPerfectNC_000015.9:g.4096
    9744_41104339dup
    GRCh37.p13First PassNC_000015.9Chr1540,969,74441,104,339

    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)
    nssv186187274e-061275832
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