A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5803665



Internal ID8781068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3627845..3631002hg38UCSC Ensembl
chr11:3649075..3652232hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383158
hg193158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663595
Supporting Variants
SamplesNA18544
Known GenesTRPC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5803665
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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