A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15210841



Internal ID5212657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34429035..34544625hg38UCSC Ensembl
chr15:34721236..34836826hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38115591
hg19115591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636115
Supporting Variants
SamplesHG03419
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15210841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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