A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665589



Internal ID9585008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105057308..105057452hg38UCSC Ensembl
chr14:105523645..105523789hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5690836
SamplesHG00734
Known GenesGPR132
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665589
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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