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nsv7060254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,327

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 16 studies. See in: genome view    
    Submitted genomic34,732,670-34,733,996Question Mark
    Overlapping variant regions from other studies: 161 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):32,312,634-32,313,960Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1834,732,67034,733,996
    nsv7060254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1832,312,63432,313,960

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757785inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757785Submitted genomicNC_000018.10:g.347
    32670_34733996inv
    GRCh38 (hg38)NC_000018.10Chr1834,732,67034,733,996
    nssv18757785RemappedPerfectNC_000018.9:g.3231
    2634_32313960inv
    GRCh37.p13First PassNC_000018.9Chr1832,312,63432,313,960

    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)
    nssv187577854e-061276268
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