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nsv6565343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,874,862

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 22351 SVs from 125 studies. See in: genome view    
    Submitted genomic32,527,987-37,402,848Question Mark
    Overlapping variant regions from other studies: 22352 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):32,495,764-37,370,624Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6565343Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr632,527,98737,402,848
    nsv6565343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr632,495,76437,370,624

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18270587inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18270587Submitted genomicNC_000006.12:g.325
    27987_37402848inv
    GRCh38 (hg38)NC_000006.12Chr632,527,98737,402,848
    nssv18270587RemappedPerfectNC_000006.11:g.324
    95764_37370624inv
    GRCh37.p13First PassNC_000006.11Chr632,495,76437,370,624

    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)
    nssv182705870.00512326266
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