A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6155428



Internal ID9132831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120516931..120517657hg38UCSC Ensembl
chr11:120387640..120388366hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666173
Supporting Variants
SamplesNA19451
Known GenesGRIK4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6155428
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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