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nsv6813246

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,164

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 16 studies. See in: genome view    
    Submitted genomic138,730,100-138,732,263Question Mark
    Overlapping variant regions from other studies: 94 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):139,051,237-139,053,400Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6813246Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6138,730,100138,732,263
    nsv6813246RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6139,051,237139,053,400

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18521184deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18521184Submitted genomicNC_000006.12:g.138
    730100_138732263de
    l
    GRCh38 (hg38)NC_000006.12Chr6138,730,100138,732,263
    nssv18521184RemappedPerfectNC_000006.11:g.139
    051237_139053400de
    l
    GRCh37.p13First PassNC_000006.11Chr6139,051,237139,053,400

    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)
    nssv18521184<0.00182252976
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