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nsv7070435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,921

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 36 studies. See in: genome view    
    Submitted genomic120,013,623-120,021,543Question Mark
    Overlapping variant regions from other studies: 111 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):120,451,427-120,459,347Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,013,623120,021,543
    nsv7070435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,451,427120,459,347

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751262inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751262Submitted genomicNC_000012.12:g.120
    013623_120021543in
    v
    GRCh38 (hg38)NC_000012.12Chr12120,013,623120,021,543
    nssv18751262RemappedPerfectNC_000012.11:g.120
    451427_120459347in
    v
    GRCh37.p13First PassNC_000012.11Chr12120,451,427120,459,347

    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)
    nssv187512624e-061276268
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