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nsv7069070

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66,174

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 217 SVs from 47 studies. See in: genome view    
    Submitted genomic92,131,674-92,197,847Question Mark
    Overlapping variant regions from other studies: 217 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):94,893,956-94,960,129Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069070Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,131,67492,197,847
    nsv7069070RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr994,893,95694,960,129

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785843inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785843Submitted genomicNC_000009.12:g.921
    31674_92197847inv
    GRCh38 (hg38)NC_000009.12Chr992,131,67492,197,847
    nssv18785843RemappedPerfectNC_000009.11:g.948
    93956_94960129inv
    GRCh37.p13First PassNC_000009.11Chr994,893,95694,960,129

    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)
    nssv18785843<0.001250270090
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