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nsv6927920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,215

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 25 studies. See in: genome view    
    Submitted genomic62,589,043-62,592,257Question Mark
    Overlapping variant regions from other studies: 113 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):62,982,823-62,986,037Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6927920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1262,589,04362,592,257
    nsv6927920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1262,982,82362,986,037

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371680deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371680Submitted genomicNC_000012.12:g.625
    89043_62592257del
    GRCh38 (hg38)NC_000012.12Chr1262,589,04362,592,257
    nssv18371680RemappedPerfectNC_000012.11:g.629
    82823_62986037del
    GRCh37.p13First PassNC_000012.11Chr1262,982,82362,986,037

    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)
    nssv183716804e-061275876
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