A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5608393



Internal ID9450571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66136193..66137250hg38UCSC Ensembl
chr11:65903664..65904721hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668639
Supporting Variants
SamplesNA18870
Known GenesPACS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5608393
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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