A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543371



Internal ID18744447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38077693..38080411hg38UCSC Ensembl
Outerchr8:38077560..38080756hg38UCSC Ensembl
Innerchr8:37935211..37937929hg19UCSC Ensembl
Outerchr8:37935078..37938274hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383197
hg193197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742118
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543371
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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