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nsv6650965

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:138,993

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 372 SVs from 58 studies. See in: genome view    
    Submitted genomic48,276,809-48,415,801Question Mark
    Overlapping variant regions from other studies: 372 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):48,742,481-48,881,473Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6650965Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr148,276,80948,415,801
    nsv6650965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr148,742,48148,881,473

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628323duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628323Submitted genomicNC_000001.11:g.482
    76809_48415801dup
    GRCh38 (hg38)NC_000001.11Chr148,276,80948,415,801
    nssv18628323RemappedPerfectNC_000001.10:g.487
    42481_48881473dup
    GRCh37.p13First PassNC_000001.10Chr148,742,48148,881,473

    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)
    nssv186283234e-061275042
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