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nsv7039602

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,582

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 29 studies. See in: genome view    
    Submitted genomic174,719,305-174,741,886Question Mark
    Overlapping variant regions from other studies: 198 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):175,584,033-175,606,614Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039602Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2174,719,305174,741,886
    nsv7039602RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2175,584,033175,606,614

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768716inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768716Submitted genomicNC_000002.12:g.174
    719305_174741886in
    v
    GRCh38 (hg38)NC_000002.12Chr2174,719,305174,741,886
    nssv18768716RemappedPerfectNC_000002.11:g.175
    584033_175606614in
    v
    GRCh37.p13First PassNC_000002.11Chr2175,584,033175,606,614

    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)
    nssv187687164e-061276268
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