A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3346571



Internal ID15193553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98000718..98001416hg38UCSC Ensembl
Innerchr15:98000717..98001417hg38UCSC Ensembl
chr15:98543948..98544646hg19UCSC Ensembl
Innerchr15:98543947..98544647hg19UCSC Ensembl
chr15:96344952..96345650hg18UCSC Ensembl
Innerchr15:96345651..96344951hg18UCSC Ensembl
Outerchr15:96343952..96346650hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689821
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3346571
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