A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14215488



Internal ID579903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79297276..79325238hg38UCSC Ensembl
chr11:79008321..79036283hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3827963
hg1927963
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626915
Supporting Variants
SamplesHG00255
Known GenesTENM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14215488
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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