A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636765



Internal ID7023559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66128771..66137439hg38UCSC Ensembl
chr15:66421109..66429777hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388669
hg198669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15272913
SamplesHG03727
Known GenesMEGF11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636765
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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