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nsv6947437

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:129

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 321 SVs from 52 studies. See in: genome view    
    Submitted genomic113,812,804-113,812,932Question Mark
    Overlapping variant regions from other studies: 325 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):114,515,777-114,515,905Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6947437Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13113,812,804113,812,932
    nsv6947437RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13114,515,777114,515,905

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18599324duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18599324Submitted genomicNC_000013.11:g.113
    812804_113812932du
    p
    GRCh38 (hg38)NC_000013.11Chr13113,812,804113,812,932
    nssv18599324RemappedPerfectNC_000013.10:g.114
    515777_114515905du
    p
    GRCh37.p13First PassNC_000013.10Chr13114,515,777114,515,905

    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)
    nssv185993240.22231796143948
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