A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14089286



Internal ID4978433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34408316..34410468hg38UCSC Ensembl
Innerchr11:34408339..34410446hg38UCSC Ensembl
Outerchr11:34408294..34410491hg38UCSC Ensembl
chr11:34429863..34432015hg19UCSC Ensembl
Innerchr11:34429886..34431993hg19UCSC Ensembl
Outerchr11:34429841..34432038hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382153
hg192153
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625911
Supporting Variants
SamplesNA12889
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14089286
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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