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nsv6792931

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,961

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 49 studies. See in: genome view    
    Submitted genomic29,995,201-30,020,161Question Mark
    Overlapping variant regions from other studies: 198 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):29,962,978-29,987,938Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6792931Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr629,995,20130,020,161
    nsv6792931RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,962,97829,987,938

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18524535deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18524535Submitted genomicNC_000006.12:g.299
    95201_30020161del
    GRCh38 (hg38)NC_000006.12Chr629,995,20130,020,161
    nssv18524535RemappedPerfectNC_000006.11:g.299
    62978_29987938del
    GRCh37.p13First PassNC_000006.11Chr629,962,97829,987,938

    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)
    nssv185245351.4e-054276054
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