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nsv6904389

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 39 studies. See in: genome view    
    Submitted genomic11,859,501-11,867,700Question Mark
    Overlapping variant regions from other studies: 112 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):11,881,048-11,889,247Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6904389Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1111,859,50111,867,700
    nsv6904389RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1111,881,04811,889,247

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18574571duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18574571Submitted genomicNC_000011.10:g.118
    59501_11867700dup
    GRCh38 (hg38)NC_000011.10Chr1111,859,50111,867,700
    nssv18574571RemappedPerfectNC_000011.9:g.1188
    1048_11889247dup
    GRCh37.p13First PassNC_000011.9Chr1111,881,04811,889,247

    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)
    nssv185745714e-061275332
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