A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14241814



Internal ID4243630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94227384..94363858hg38UCSC Ensembl
chr11:93960550..94097024hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38136475
hg19136475
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627315
Supporting Variants
SamplesHG04006
Known GenesFOLR4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14241814
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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