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nsv7055010

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,231

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 218 SVs from 26 studies. See in: genome view    
    Submitted genomic238,083,620-238,090,850Question Mark
    Overlapping variant regions from other studies: 218 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):238,992,261-238,999,491Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055010Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2238,083,620238,090,850
    nsv7055010RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,992,261238,999,491

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767820inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767820Submitted genomicNC_000002.12:g.238
    083620_238090850in
    v
    GRCh38 (hg38)NC_000002.12Chr2238,083,620238,090,850
    nssv18767820RemappedPerfectNC_000002.11:g.238
    992261_238999491in
    v
    GRCh37.p13First PassNC_000002.11Chr2238,992,261238,999,491

    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)
    nssv187678207e-062274650
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