A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3386077



Internal ID15233047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22530987..22536985hg38UCSC Ensembl
Innerchr15:22531987..22535985hg38UCSC Ensembl
Outerchr15:22529987..22537985hg38UCSC Ensembl
chr15:23336111..23342109hg19UCSC Ensembl
Innerchr15:23337111..23341109hg19UCSC Ensembl
Outerchr15:23335111..23343109hg19UCSC Ensembl
chr15:20887552..20893550hg18UCSC Ensembl
Innerchr15:20888552..20892550hg18UCSC Ensembl
Outerchr15:20886552..20894550hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385999
hg195999
hg185999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689683
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3386077
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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