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nsv6960107

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:124,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 444 SVs from 51 studies. See in: genome view    
    Submitted genomic88,742,701-88,867,100Question Mark
    Overlapping variant regions from other studies: 444 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):89,209,045-89,333,444Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960107Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1488,742,70188,867,100
    nsv6960107RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1489,209,04589,333,444

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615225duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615225Submitted genomicNC_000014.9:g.8874
    2701_88867100dup
    GRCh38 (hg38)NC_000014.9Chr1488,742,70188,867,100
    nssv18615225RemappedPerfectNC_000014.8:g.8920
    9045_89333444dup
    GRCh37.p13First PassNC_000014.8Chr1489,209,04589,333,444

    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)
    nssv186152254e-061275380
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