A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660789



Internal ID9580208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73857178..73861177hg38UCSC Ensembl
chr14:74323881..74327880hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5479268
SamplesNA19462
Known GenesPTGR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660789
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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