A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6384615



Internal ID9362018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65842768..65843041hg38UCSC Ensembl
chr11:65610239..65610512hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662850
Supporting Variants
SamplesNA18612
Known GenesSNX32
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6384615
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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