A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634874



Internal ID7021674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71179095..71189700hg38UCSC Ensembl
chr14:71645812..71656417hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3810606
hg1910606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15053932
SamplesNA20888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634874
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