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nsv7068624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,872,536

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7680 SVs from 112 studies. See in: genome view    
    Submitted genomic2,500,360-5,372,895Question Mark
    Overlapping variant regions from other studies: 7680 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):2,609,526-5,482,061Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr122,500,3605,372,895
    nsv7068624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr122,609,5265,482,061

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751710inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751710Submitted genomicNC_000012.12:g.250
    0360_5372895inv
    GRCh38 (hg38)NC_000012.12Chr122,500,3605,372,895
    nssv18751710RemappedPerfectNC_000012.11:g.260
    9526_5482061inv
    GRCh37.p13First PassNC_000012.11Chr122,609,5265,482,061

    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)
    nssv187517104e-061276268
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