A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674194



Internal ID9940299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20008756..20021376hg38UCSC Ensembl
chr14:20476915..20489535hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3812621
hg1912621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5409803
SamplesNA20531
Known GenesOR4K14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674194
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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