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nsv7043011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic33,664,125-33,664,189Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):34,129,725-34,129,789Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,664,12533,664,189
    nsv7043011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr134,129,72534,129,789

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760313inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760313Submitted genomicNC_000001.11:g.336
    64125_33664189inv
    GRCh38 (hg38)NC_000001.11Chr133,664,12533,664,189
    nssv18760313RemappedPerfectNC_000001.10:g.341
    29725_34129789inv
    GRCh37.p13First PassNC_000001.10Chr134,129,72534,129,789

    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)
    nssv187603134e-061276254
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