A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742615



Internal ID18716861
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 StatusS
Merged Variantsesv3543868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742615
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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