A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689687



Internal ID15094500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22515887..22527685hg38UCSC Ensembl
Innerchr15:22516887..22526685hg38UCSC Ensembl
Outerchr15:22514887..22528685hg38UCSC Ensembl
chr15:23345411..23357209hg19UCSC Ensembl
Innerchr15:23346411..23356209hg19UCSC Ensembl
Outerchr15:23344411..23358209hg19UCSC Ensembl
chr15:20896852..20908650hg18UCSC Ensembl
Innerchr15:20897852..20907650hg18UCSC Ensembl
Outerchr15:20895852..20909650hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811799
hg1911799
hg1811799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3430595
Supporting Variants
SamplesNA19240
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689687
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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