A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635620



Internal ID7022419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104230962..104422836hg38UCSC Ensembl
chr14:104697299..104889173hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38191875
hg19191875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15114698, essv15114700, essv15114699
SamplesNA06984, HG00266, HG00186
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635620
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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