A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15230569



Internal ID5232385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41301141..41325158hg38UCSC Ensembl
chr15:41593339..41617356hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3824018
hg1924018
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636241
Supporting Variants
SamplesHG02154
Known GenesOIP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15230569
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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