A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14343361



Internal ID22196726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114504412..114585979hg38UCSC Ensembl
chr8:115516641..115598208hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3881568
hg1981568
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3242366
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14343361
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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