A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3399428



Internal ID15246391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22525087..22529985hg38UCSC Ensembl
Innerchr15:22526087..22528985hg38UCSC Ensembl
Outerchr15:22524087..22530985hg38UCSC Ensembl
chr15:23343111..23348009hg19UCSC Ensembl
Innerchr15:23344111..23347009hg19UCSC Ensembl
Outerchr15:23342111..23349009hg19UCSC Ensembl
chr15:20894552..20899450hg18UCSC Ensembl
Innerchr15:20895552..20898450hg18UCSC Ensembl
Outerchr15:20893552..20900450hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384899
hg194899
hg184899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689684
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3399428
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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