A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3410031



Internal ID15256991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20465385..20480283hg38UCSC Ensembl
Innerchr15:20466385..20479283hg38UCSC Ensembl
Outerchr15:20464385..20481283hg38UCSC Ensembl
chr15:20670638..20685536hg19UCSC Ensembl
Innerchr15:20671638..20684536hg19UCSC Ensembl
Outerchr15:20669638..20686536hg19UCSC Ensembl
chr15:18930652..18945550hg18UCSC Ensembl
Innerchr15:18931652..18944550hg18UCSC Ensembl
Outerchr15:18929652..18946550hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3814899
hg1914899
hg1814899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689563
SamplesNA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3410031
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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