A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636496



Internal ID7023290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52829161..52830876hg38UCSC Ensembl
Innerchr15:52829161..52830876hg38UCSC Ensembl
Outerchr15:52828898..52831040hg38UCSC Ensembl
chr15:53121358..53123073hg19UCSC Ensembl
Innerchr15:53121358..53123073hg19UCSC Ensembl
Outerchr15:53121095..53123237hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381716
hg191716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15249435
SamplesNA19678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636496
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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