nsv6994896

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,956

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 36 studies. See in: genome view    
    Submitted genomic39,480,193-39,483,148Question Mark
    Overlapping variant regions from other studies: 162 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):37,636,446-37,639,401Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6994896Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,480,19339,483,148
    nsv6994896RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1737,636,44637,639,401

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18407947deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18407947Submitted genomicNC_000017.11:g.394
    80193_39483148del
    GRCh38 (hg38)NC_000017.11Chr1739,480,19339,483,148
    nssv18407947RemappedPerfectNC_000017.10:g.376
    36446_37639401del
    GRCh37.p13First PassNC_000017.10Chr1737,636,44637,639,401

    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)
    nssv184079471.1e-053272948
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