A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5711715



Internal ID9298222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25008763..25038636hg38UCSC Ensembl
Outerchr11:25008726..25038686hg38UCSC Ensembl
Innerchr11:25030309..25060182hg19UCSC Ensembl
Outerchr11:25030272..25060232hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3829961
hg1929961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658856
Supporting Variants
SamplesNA12889
Known GenesLUZP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5711715
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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