A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5805696



Internal ID9185963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105894779..105895098hg38UCSC Ensembl
chr11:105765505..105765824hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658816
Supporting Variants
SamplesHG01456
Known GenesGRIA4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5805696
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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