A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642132



Internal ID7028902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31706537..31710896hg38UCSC Ensembl
Innerchr18:31706548..31710885hg38UCSC Ensembl
Outerchr18:31706526..31710907hg38UCSC Ensembl
chr18:29286500..29290859hg19UCSC Ensembl
Innerchr18:29286511..29290848hg19UCSC Ensembl
Outerchr18:29286489..29290870hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg384360
hg194360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15837694
SamplesHG03960
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642132
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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