A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636149



Internal ID7022945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36077767..36094504hg38UCSC Ensembl
chr15:36369968..36386705hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3816738
hg1916738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15216362
SamplesHG04239
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636149
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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