A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633864



Internal ID7020670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26997110..27061804hg38UCSC Ensembl
chr14:27466316..27531010hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3864695
hg1964695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14946922, essv14946921
SamplesHG02070, HG02406
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633864
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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