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nsv6764171

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:181,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 675 SVs from 62 studies. See in: genome view    
    Submitted genomic55,338,901-55,520,300Question Mark
    Overlapping variant regions from other studies: 675 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):54,634,729-54,816,128Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6764171Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr555,338,90155,520,300
    nsv6764171RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr554,634,72954,816,128

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18705326duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18705326Submitted genomicNC_000005.10:g.553
    38901_55520300dup
    GRCh38 (hg38)NC_000005.10Chr555,338,90155,520,300
    nssv18705326RemappedPerfectNC_000005.9:g.5463
    4729_54816128dup
    GRCh37.p13First PassNC_000005.9Chr554,634,72954,816,128

    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)
    nssv187053263.9e-0511273828
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