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nsv6737996

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 188 SVs from 29 studies. See in: genome view    
    Submitted genomic172,380,201-172,425,000Question Mark
    Overlapping variant regions from other studies: 188 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):172,097,991-172,142,790Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737996Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3172,380,201172,425,000
    nsv6737996RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3172,097,991172,142,790

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18674003duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18674003Submitted genomicNC_000003.12:g.172
    380201_172425000du
    p
    GRCh38 (hg38)NC_000003.12Chr3172,380,201172,425,000
    nssv18674003RemappedPerfectNC_000003.11:g.172
    097991_172142790du
    p
    GRCh37.p13First PassNC_000003.11Chr3172,097,991172,142,790

    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)
    nssv186740033.2e-059271838
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