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nsv6953234

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,298,660

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3519 SVs from 98 studies. See in: genome view    
    Submitted genomic49,610,822-50,909,481Question Mark
    Overlapping variant regions from other studies: 3519 SVs from 98 studies. See in: genome view    
    Remapped(Score: Perfect):50,184,958-51,483,617Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6953234Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1349,610,82250,909,481
    nsv6953234RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1350,184,95851,483,617

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18377994deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18377994Submitted genomicNC_000013.11:g.496
    10822_50909481del
    GRCh38 (hg38)NC_000013.11Chr1349,610,82250,909,481
    nssv18377994RemappedPerfectNC_000013.10:g.501
    84958_51483617del
    GRCh37.p13First PassNC_000013.10Chr1350,184,95851,483,617

    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)
    nssv183779944e-061275880
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