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nsv6879681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 183 SVs from 37 studies. See in: genome view    
    Submitted genomic49,125,133-49,125,214Question Mark
    Overlapping variant regions from other studies: 182 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):50,333,178-50,333,259Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6879681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1049,125,13349,125,214
    nsv6879681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1050,333,17850,333,259

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18336773deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18336773Submitted genomicNC_000010.11:g.491
    25133_49125214del
    GRCh38 (hg38)NC_000010.11Chr1049,125,13349,125,214
    nssv18336773RemappedPerfectNC_000010.10:g.503
    33178_50333259del
    GRCh37.p13First PassNC_000010.10Chr1050,333,17850,333,259

    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)
    nssv18336773<0.00143250828
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