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nsv6935054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:902

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
    Submitted genomic9,902,670-9,903,571Question Mark
    Overlapping variant regions from other studies: 126 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):10,055,269-10,056,170Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6935054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,902,6709,903,571
    nsv6935054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,055,26910,056,170

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18599092duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18599092Submitted genomicNC_000012.12:g.990
    2670_9903571dup
    GRCh38 (hg38)NC_000012.12Chr129,902,6709,903,571
    nssv18599092RemappedPerfectNC_000012.11:g.100
    55269_10056170dup
    GRCh37.p13First PassNC_000012.11Chr1210,055,26910,056,170

    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)
    nssv185990923e-058257076
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