A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634955



Internal ID7021755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75165714..75195959hg38UCSC Ensembl
chr14:75632417..75662662hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3830246
hg1930246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15063982
SamplesHG01974
Known GenesTMED10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634955
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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