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nsv6796826

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 167 SVs from 39 studies. See in: genome view    
    Submitted genomic24,302,501-24,324,500Question Mark
    Overlapping variant regions from other studies: 167 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):24,302,729-24,324,728Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6796826Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr624,302,50124,324,500
    nsv6796826RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr624,302,72924,324,728

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18524245deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18524245Submitted genomicNC_000006.12:g.243
    02501_24324500del
    GRCh38 (hg38)NC_000006.12Chr624,302,50124,324,500
    nssv18524245RemappedPerfectNC_000006.11:g.243
    02729_24324728del
    GRCh37.p13First PassNC_000006.11Chr624,302,72924,324,728

    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)
    nssv185242454e-061245188
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