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nsv6988876

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 17 studies. See in: genome view    
    Submitted genomic43,651,946-43,651,977Question Mark
    Overlapping variant regions from other studies: 146 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):41,729,314-41,729,345Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6988876Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1743,651,94643,651,977
    nsv6988876RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,729,31441,729,345

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18411477deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18411477Submitted genomicNC_000017.11:g.436
    51946_43651977del
    GRCh38 (hg38)NC_000017.11Chr1743,651,94643,651,977
    nssv18411477RemappedPerfectNC_000017.10:g.417
    29314_41729345del
    GRCh37.p13First PassNC_000017.10Chr1741,729,31441,729,345

    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)
    nssv184114770.001377259032
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