A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15270948



Internal ID5272764
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636712
Supporting Variants
SamplesNA19225
Known GenesLACTB, RAB8B, RPS27L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15270948
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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