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nsv6785251

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:181,662

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 853 SVs from 85 studies. See in: genome view    
    Submitted genomic35,599,467-35,781,128Question Mark
    Overlapping variant regions from other studies: 853 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):35,567,244-35,748,905Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785251Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr635,599,46735,781,128
    nsv6785251RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr635,567,24435,748,905

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18712909duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18712909Submitted genomicNC_000006.12:g.355
    99467_35781128dup
    GRCh38 (hg38)NC_000006.12Chr635,599,46735,781,128
    nssv18712909RemappedPerfectNC_000006.11:g.355
    67244_35748905dup
    GRCh37.p13First PassNC_000006.11Chr635,567,24435,748,905

    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)
    nssv187129094e-061275460
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