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nsv6752236

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,692

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 337 SVs from 59 studies. See in: genome view    
    Submitted genomic68,027,016-68,073,707Question Mark
    Overlapping variant regions from other studies: 337 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):68,892,734-68,939,425Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6752236Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,027,01668,073,707
    nsv6752236RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,892,73468,939,425

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692638duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692638Submitted genomicNC_000004.12:g.680
    27016_68073707dup
    GRCh38 (hg38)NC_000004.12Chr468,027,01668,073,707
    nssv18692638RemappedPerfectNC_000004.11:g.688
    92734_68939425dup
    GRCh37.p13First PassNC_000004.11Chr468,892,73468,939,425

    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)
    nssv186926387e-062275520
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