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nsv6353445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:455

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 20 studies. See in: genome view    
    Submitted genomic176,300,699-176,301,153Question Mark
    Overlapping variant regions from other studies: 169 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):177,165,427-177,165,881Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6353445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2176,300,699176,301,153
    nsv6353445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2177,165,427177,165,881

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18082043deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18082043Submitted genomicNC_000002.12:g.176
    300699_176301153de
    l
    GRCh38 (hg38)NC_000002.12Chr2176,300,699176,301,153
    nssv18082043RemappedPerfectNC_000002.11:g.177
    165427_177165881de
    l
    GRCh37.p13First PassNC_000002.11Chr2177,165,427177,165,881

    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)
    nssv18082043<0.0012237126
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