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nsv6957279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 20 studies. See in: genome view    
    Submitted genomic51,945,244-51,945,391Question Mark
    Overlapping variant regions from other studies: 157 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):52,519,380-52,519,527Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6957279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1351,945,24451,945,391
    nsv6957279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,519,38052,519,527

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18601737duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18601737Submitted genomicNC_000013.11:g.519
    45244_51945391dup
    GRCh38 (hg38)NC_000013.11Chr1351,945,24451,945,391
    nssv18601737RemappedPerfectNC_000013.10:g.525
    19380_52519527dup
    GRCh37.p13First PassNC_000013.10Chr1352,519,38052,519,527

    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)
    nssv18601737<0.00119232382
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