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nsv7048862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,230

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 48 studies. See in: genome view    
    Submitted genomic160,230,887-160,238,116Question Mark
    Overlapping variant regions from other studies: 159 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):160,651,919-160,659,148Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048862Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6160,230,887160,238,116
    nsv7048862RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,651,919160,659,148

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777579inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777579Submitted genomicNC_000006.12:g.160
    230887_160238116in
    v
    GRCh38 (hg38)NC_000006.12Chr6160,230,887160,238,116
    nssv18777579RemappedPerfectNC_000006.11:g.160
    651919_160659148in
    v
    GRCh37.p13First PassNC_000006.11Chr6160,651,919160,659,148

    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)
    nssv187775797e-062274418
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