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nsv7076223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:221,731

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 802 SVs from 69 studies. See in: genome view    
    Submitted genomic132,900,540-133,122,270Question Mark
    Overlapping variant regions from other studies: 802 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):133,477,126-133,698,856Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12132,900,540133,122,270
    nsv7076223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,477,126133,698,856

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752170inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752170Submitted genomicNC_000012.12:g.132
    900540_133122270in
    v
    GRCh38 (hg38)NC_000012.12Chr12132,900,540133,122,270
    nssv18752170RemappedPerfectNC_000012.11:g.133
    477126_133698856in
    v
    GRCh37.p13First PassNC_000012.11Chr12133,477,126133,698,856

    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)
    nssv187521703.9e-0511273924
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