A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5566568



Internal ID9696731
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 Flag1
Merged StatusS
Merged Variantsesv2662365
Supporting Variants
SamplesNA19446
Known GenesCLDN16, TMEM207
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5566568
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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