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nsv6666198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,094

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 373 SVs from 45 studies. See in: genome view    
    Submitted genomic203,760,911-203,833,004Question Mark
    Overlapping variant regions from other studies: 373 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):203,730,039-203,802,132Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6666198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1203,760,911203,833,004
    nsv6666198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1203,730,039203,802,132

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18605805duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18605805Submitted genomicNC_000001.11:g.203
    760911_203833004du
    p
    GRCh38 (hg38)NC_000001.11Chr1203,760,911203,833,004
    nssv18605805RemappedPerfectNC_000001.10:g.203
    730039_203802132du
    p
    GRCh37.p13First PassNC_000001.10Chr1203,730,039203,802,132

    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)
    nssv186058054e-061275684
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