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nsv6736202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,070,151

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4208 SVs from 115 studies. See in: genome view    
    Submitted genomic9,649,300-10,719,450Question Mark
    Overlapping variant regions from other studies: 4208 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):9,650,924-10,721,074Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6736202Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr49,649,30010,719,450
    nsv6736202RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr49,650,92410,721,074

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18695223duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18695223Submitted genomicNC_000004.12:g.964
    9300_10719450dup
    GRCh38 (hg38)NC_000004.12Chr49,649,30010,719,450
    nssv18695223RemappedPerfectNC_000004.11:g.965
    0924_10721074dup
    GRCh37.p13First PassNC_000004.11Chr49,650,92410,721,074

    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)
    nssv186952234e-061272188
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