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nsv6996858

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109,557

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 648 SVs from 61 studies. See in: genome view    
    Submitted genomic84,311,970-84,421,526Question Mark
    Overlapping variant regions from other studies: 648 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):84,345,576-84,455,132Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6996858Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,311,97084,421,526
    nsv6996858RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,345,57684,455,132

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624080duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624080Submitted genomicNC_000016.10:g.843
    11970_84421526dup
    GRCh38 (hg38)NC_000016.10Chr1684,311,97084,421,526
    nssv18624080RemappedPerfectNC_000016.9:g.8434
    5576_84455132dup
    GRCh37.p13First PassNC_000016.9Chr1684,345,57684,455,132

    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)
    nssv186240807e-062273760
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