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nsv6669439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,565

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Submitted genomic212,965,261-212,969,825Question Mark
    Overlapping variant regions from other studies: 136 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):213,138,603-213,143,167Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6669439Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1212,965,261212,969,825
    nsv6669439RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1213,138,603213,143,167

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18366573deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18366573Submitted genomicNC_000001.11:g.212
    965261_212969825de
    l
    GRCh38 (hg38)NC_000001.11Chr1212,965,261212,969,825
    nssv18366573RemappedPerfectNC_000001.10:g.213
    138603_213143167de
    l
    GRCh37.p13First PassNC_000001.10Chr1213,138,603213,143,167

    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)
    nssv183665734e-061276194
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