A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616531



Internal ID6656727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18933336..18935012hg38UCSC Ensembl
Innerchr8:18933386..18934962hg38UCSC Ensembl
Outerchr8:18933282..18935066hg38UCSC Ensembl
chr8:18790846..18792522hg19UCSC Ensembl
Innerchr8:18790896..18792472hg19UCSC Ensembl
Outerchr8:18790792..18792576hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13130960
SamplesHG04155
Known GenesPSD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616531
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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