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nsv6708929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 31 studies. See in: genome view    
    Submitted genomic11,796,501-11,798,700Question Mark
    Overlapping variant regions from other studies: 106 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):11,837,975-11,840,174Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6708929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,796,50111,798,700
    nsv6708929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,837,97511,840,174

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18670189duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18670189Submitted genomicNC_000003.12:g.117
    96501_11798700dup
    GRCh38 (hg38)NC_000003.12Chr311,796,50111,798,700
    nssv18670189RemappedPerfectNC_000003.11:g.118
    37975_11840174dup
    GRCh37.p13First PassNC_000003.11Chr311,837,97511,840,174

    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)
    nssv186701897e-062270458
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