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nsv6799999

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:651,828

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1320 SVs from 73 studies. See in: genome view    
    Submitted genomic139,637,430-140,289,257Question Mark
    Overlapping variant regions from other studies: 1320 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):139,958,567-140,610,394Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6799999Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6139,637,430140,289,257
    nsv6799999RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6139,958,567140,610,394

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18707381duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18707381Submitted genomicNC_000006.12:g.139
    637430_140289257du
    p
    GRCh38 (hg38)NC_000006.12Chr6139,637,430140,289,257
    nssv18707381RemappedPerfectNC_000006.11:g.139
    958567_140610394du
    p
    GRCh37.p13First PassNC_000006.11Chr6139,958,567140,610,394

    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)
    nssv187073814e-061273694
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