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nsv6732977

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:427

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 26 studies. See in: genome view    
    Submitted genomic177,171,107-177,171,533Question Mark
    Overlapping variant regions from other studies: 134 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):176,888,895-176,889,321Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6732977Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3177,171,107177,171,533
    nsv6732977RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3176,888,895176,889,321

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18477147deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18477147Submitted genomicNC_000003.12:g.177
    171107_177171533de
    l
    GRCh38 (hg38)NC_000003.12Chr3177,171,107177,171,533
    nssv18477147RemappedPerfectNC_000003.11:g.176
    888895_176889321de
    l
    GRCh37.p13First PassNC_000003.11Chr3176,888,895176,889,321

    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)
    nssv184771474e-061261744
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