A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317796



Internal ID4319612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133065549..133100485hg38UCSC Ensembl
chr11:132935444..132970380hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3834937
hg1934937
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628137
Supporting Variants
SamplesHG01308
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317796
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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