A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5776235



Internal ID9673333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9225120..9225455hg38UCSC Ensembl
chr18:9225118..9225453hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676874
Supporting Variants
SamplesNA19403
Known GenesANKRD12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5776235
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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