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nsv7047988

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 22 studies. See in: genome view    
    Submitted genomic156,139,085-156,139,165Question Mark
    Overlapping variant regions from other studies: 127 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):156,995,597-156,995,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047988Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2156,139,085156,139,165
    nsv7047988RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2156,995,597156,995,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766036inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766036Submitted genomicNC_000002.12:g.156
    139085_156139165in
    v
    GRCh38 (hg38)NC_000002.12Chr2156,139,085156,139,165
    nssv18766036RemappedPerfectNC_000002.11:g.156
    995597_156995677in
    v
    GRCh37.p13First PassNC_000002.11Chr2156,995,597156,995,677

    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)
    nssv187660364e-061276116
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