A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7731875



Internal ID14684552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90483822..90483823hg38UCSC Ensembl
Outerchr14:90483642..90484003hg38UCSC Ensembl
Innerchr14:90950166..90950167hg19UCSC Ensembl
Outerchr14:90949986..90950347hg19UCSC Ensembl
Innerchr14:90019920..90019919hg18UCSC Ensembl
Outerchr14:90019739..90020100hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38362
hg19362
hg18362
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302791
Supporting Variants
SamplesNA18965
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7731875
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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