A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3377517



Internal ID15224490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22516687..22524185hg38UCSC Ensembl
Innerchr15:22517687..22523185hg38UCSC Ensembl
Outerchr15:22515687..22525185hg38UCSC Ensembl
chr15:23348911..23356409hg19UCSC Ensembl
Innerchr15:23349911..23355409hg19UCSC Ensembl
Outerchr15:23347911..23357409hg19UCSC Ensembl
chr15:20900352..20907850hg18UCSC Ensembl
Innerchr15:20901352..20906850hg18UCSC Ensembl
Outerchr15:20899352..20908850hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387499
hg197499
hg187499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689689
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3377517
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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