A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3364198



Internal ID15211176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22502587..22509585hg38UCSC Ensembl
Innerchr15:22503587..22508585hg38UCSC Ensembl
Outerchr15:22501587..22510585hg38UCSC Ensembl
chr15:23363511..23370509hg19UCSC Ensembl
Innerchr15:23364511..23369509hg19UCSC Ensembl
Outerchr15:23362511..23371509hg19UCSC Ensembl
chr15:20914952..20921950hg18UCSC Ensembl
Innerchr15:20915952..20920950hg18UCSC Ensembl
Outerchr15:20913952..20922950hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386999
hg196999
hg186999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689694
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3364198
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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