A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5823138



Internal ID8800541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854051..11855011hg38UCSC Ensembl
chr11:11875598..11876558hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668480
Supporting Variants
SamplesHG00608
Known GenesUSP47
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5823138
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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