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nsv6930863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 21 studies. See in: genome view    
    Submitted genomic16,840,101-16,840,245Question Mark
    Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):16,993,035-16,993,179Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1216,840,10116,840,245
    nsv6930863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1216,993,03516,993,179

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18592902duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18592902Submitted genomicNC_000012.12:g.168
    40101_16840245dup
    GRCh38 (hg38)NC_000012.12Chr1216,840,10116,840,245
    nssv18592902RemappedPerfectNC_000012.11:g.169
    93035_16993179dup
    GRCh37.p13First PassNC_000012.11Chr1216,993,03516,993,179

    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)
    nssv185929024e-061229326
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