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nsv7070965

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 23 studies. See in: genome view    
    Submitted genomic50,686,510-50,686,572Question Mark
    Overlapping variant regions from other studies: 125 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):51,599,070-51,599,132Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070965Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr850,686,51050,686,572
    nsv7070965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr851,599,07051,599,132

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782468inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782468Submitted genomicNC_000008.11:g.506
    86510_50686572inv
    GRCh38 (hg38)NC_000008.11Chr850,686,51050,686,572
    nssv18782468RemappedPerfectNC_000008.10:g.515
    99070_51599132inv
    GRCh37.p13First PassNC_000008.10Chr851,599,07051,599,132

    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)
    nssv18782468<0.001106274928
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