A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689691



Internal ID15054595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22510187..22514985hg38UCSC Ensembl
Innerchr15:22511187..22513985hg38UCSC Ensembl
Outerchr15:22509187..22515985hg38UCSC Ensembl
chr15:23358111..23362909hg19UCSC Ensembl
Innerchr15:23359111..23361909hg19UCSC Ensembl
Outerchr15:23357111..23363909hg19UCSC Ensembl
chr15:20909552..20914350hg18UCSC Ensembl
Innerchr15:20910552..20913350hg18UCSC Ensembl
Outerchr15:20908552..20915350hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384799
hg194799
hg184799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3447921
Supporting Variants
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689691
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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