A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5958458



Internal ID9614137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17112807..17113963hg38UCSC Ensembl
chr11:17134354..17135510hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677594
Supporting Variants
SamplesNA19316
Known GenesPIK3C2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5958458
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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