A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543868



Internal ID18744944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94712939..94715772hg38UCSC Ensembl
Outerchr8:94712773..94716077hg38UCSC Ensembl
Innerchr8:95725167..95728000hg19UCSC Ensembl
Outerchr8:95725001..95728305hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383305
hg193305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742615
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543868
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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