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nsv7038090

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,863,763

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 20387 SVs from 122 studies. See in: genome view    
    Submitted genomic152,079,952-160,943,714Question Mark
    Overlapping variant regions from other studies: 20387 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):152,936,466-161,800,225Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038090Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2152,079,952160,943,714
    nsv7038090RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2152,936,466161,800,225

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765965inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765965Submitted genomicNC_000002.12:g.152
    079952_160943714in
    v
    GRCh38 (hg38)NC_000002.12Chr2152,079,952160,943,714
    nssv18765965RemappedPerfectNC_000002.11:g.152
    936466_161800225in
    v
    GRCh37.p13First PassNC_000002.11Chr2152,936,466161,800,225

    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)
    nssv187659654e-061276268
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