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nsv6787365

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,277

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 249 SVs from 45 studies. See in: genome view    
    Submitted genomic26,428,939-26,466,215Question Mark
    Overlapping variant regions from other studies: 249 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):26,429,167-26,466,443Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787365Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,428,93926,466,215
    nsv6787365RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,429,16726,466,443

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18527872deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18527872Submitted genomicNC_000006.12:g.264
    28939_26466215del
    GRCh38 (hg38)NC_000006.12Chr626,428,93926,466,215
    nssv18527872RemappedPerfectNC_000006.11:g.264
    29167_26466443del
    GRCh37.p13First PassNC_000006.11Chr626,429,16726,466,443

    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)
    nssv18527872<0.00181253592
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