A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15344327



Internal ID5323739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99216374..99369158hg38UCSC Ensembl
chr15:99756579..99909363hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38152785
hg19152785
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637424
Supporting Variants
SamplesNA18868
Known GenesHSP90B2P, LRRC28, TTC23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15344327
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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