nsv6717272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:212

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Submitted genomic48,371,817-48,372,028Question Mark
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):48,413,307-48,413,518Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6717272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr348,371,81748,372,028
    nsv6717272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr348,413,30748,413,518

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18676544duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18676544Submitted genomicNC_000003.12:g.483
    71817_48372028dup
    GRCh38 (hg38)NC_000003.12Chr348,371,81748,372,028
    nssv18676544RemappedPerfectNC_000003.11:g.484
    13307_48413518dup
    GRCh37.p13First PassNC_000003.11Chr348,413,30748,413,518

    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)
    nssv186765444e-061237846
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