A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662365



Internal ID9928470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190396382..190433672hg38UCSC Ensembl
chr3:190114171..190151461hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3837291
hg1937291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv902e199
Supporting Variantsessv5566568
SamplesNA19446
Known GenesCLDN16, TMEM207
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662365
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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