A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635547



Internal ID6675660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102223491..102317911hg38UCSC Ensembl
chr14:102689828..102784248hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3894421
hg1994421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109389
SamplesNA06984
Known GenesMOK, WDR20, ZNF839
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635547
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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