A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636792



Internal ID7023586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67684004..67689385hg38UCSC Ensembl
Innerchr15:67684055..67689334hg38UCSC Ensembl
Outerchr15:67683953..67689436hg38UCSC Ensembl
chr15:67976342..67981723hg19UCSC Ensembl
Innerchr15:67976393..67981672hg19UCSC Ensembl
Outerchr15:67976291..67981774hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385382
hg195382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15276766
SamplesHG01808
Known GenesMAP2K5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636792
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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