A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634573



Internal ID7021376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55156562..55224270hg38UCSC Ensembl
chr14:55623280..55690988hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3867709
hg1967709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15019163, essv15019164, essv15019162
SamplesHG04222, HG03862, HG04080
Known GenesDLGAP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634573
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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