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nsv6659137

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 22 studies. See in: genome view    
    Submitted genomic47,335,790-47,335,854Question Mark
    Overlapping variant regions from other studies: 150 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):47,562,929-47,562,993Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6659137Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr247,335,79047,335,854
    nsv6659137RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr247,562,92947,562,993

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18465596deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18465596Submitted genomicNC_000002.12:g.473
    35790_47335854del
    GRCh38 (hg38)NC_000002.12Chr247,335,79047,335,854
    nssv18465596RemappedPerfectNC_000002.11:g.475
    62929_47562993del
    GRCh37.p13First PassNC_000002.11Chr247,562,92947,562,993

    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)
    nssv18465596<0.00122196882
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