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nsv6885052

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,365

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Submitted genomic15,301,613-15,312,977Question Mark
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):15,343,612-15,354,976Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6885052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1015,301,61315,312,977
    nsv6885052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1015,343,61215,354,976

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581887duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581887Submitted genomicNC_000010.11:g.153
    01613_15312977dup
    GRCh38 (hg38)NC_000010.11Chr1015,301,61315,312,977
    nssv18581887RemappedPerfectNC_000010.10:g.153
    43612_15354976dup
    GRCh37.p13First PassNC_000010.10Chr1015,343,61215,354,976

    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)
    nssv185818872.1e-056275932
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