A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696617



Internal ID15058413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37352..41150hg38UCSC Ensembl
Innerchr9:38352..40150hg38UCSC Ensembl
Outerchr9:36352..42150hg38UCSC Ensembl
chr9:37352..41150hg19UCSC Ensembl
Innerchr9:38352..40150hg19UCSC Ensembl
Outerchr9:36352..42150hg19UCSC Ensembl
chr9:27352..31150hg18UCSC Ensembl
Innerchr9:28352..30150hg18UCSC Ensembl
Outerchr9:26352..32150hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg383799
hg193799
hg183799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3449696
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696617
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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