A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634770



Internal ID7021571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65266293..65275662hg38UCSC Ensembl
chr14:65733011..65742380hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg389370
hg199370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv405e214
Supporting Variantsessv15044293, essv15044291, essv15044292
SamplesHG00626, HG00442, HG00451
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634770
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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