A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5519993



Internal ID9656842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76431283..76437507hg38UCSC Ensembl
chr11:76142327..76148551hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386225
hg196225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658544
Supporting Variants
SamplesNA19385
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5519993
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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