A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279793



Internal ID5281609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69211145..69230108hg38UCSC Ensembl
chr15:69503484..69522447hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3818964
hg1918964
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636821
Supporting Variants
SamplesNA11894
Known GenesGLCE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279793
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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