A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641564



Internal ID7028338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2634220..2643515hg38UCSC Ensembl
chr18:2634219..2643514hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg389296
hg199296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15778137
SamplesHG01624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641564
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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