A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636712



Internal ID6676819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63088307..63255422hg38UCSC Ensembl
chr15:63380506..63547621hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38167116
hg19167116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15270948
SamplesNA19225
Known GenesLACTB, RAB8B, RPS27L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636712
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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