A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689552



Internal ID15019619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20431585..20434283hg38UCSC Ensembl
Innerchr15:20432585..20433283hg38UCSC Ensembl
Outerchr15:20430585..20435283hg38UCSC Ensembl
chr15:20636838..20639536hg19UCSC Ensembl
Innerchr15:20637838..20638536hg19UCSC Ensembl
Outerchr15:20635838..20640536hg19UCSC Ensembl
chr15:18896852..18899550hg18UCSC Ensembl
Innerchr15:18897852..18898550hg18UCSC Ensembl
Outerchr15:18895852..18900550hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3430361
Supporting Variants
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689552
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer