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nsv7001813

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:516,094

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1548 SVs from 80 studies. See in: genome view    
    Submitted genomic10,003,114-10,519,207Question Mark
    Overlapping variant regions from other studies: 1548 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):10,003,111-10,519,204Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7001813Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1810,003,11410,519,207
    nsv7001813RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1810,003,11110,519,204

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18632293duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18632293Submitted genomicNC_000018.10:g.100
    03114_10519207dup
    GRCh38 (hg38)NC_000018.10Chr1810,003,11410,519,207
    nssv18632293RemappedPerfectNC_000018.9:g.1000
    3111_10519204dup
    GRCh37.p13First PassNC_000018.9Chr1810,003,11110,519,204

    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)
    nssv186322934e-061275564
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