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nsv6794164

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:424

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Submitted genomic11,202,641-11,203,064Question Mark
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):11,202,874-11,203,297Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6794164Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr611,202,64111,203,064
    nsv6794164RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr611,202,87411,203,297

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18709516duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18709516Submitted genomicNC_000006.12:g.112
    02641_11203064dup
    GRCh38 (hg38)NC_000006.12Chr611,202,64111,203,064
    nssv18709516RemappedPerfectNC_000006.11:g.112
    02874_11203297dup
    GRCh37.p13First PassNC_000006.11Chr611,202,87411,203,297

    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)
    nssv187095164e-061241690
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