A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13999297



Internal ID6663617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4795368..4846466hg38UCSC Ensembl
Innerchr11:4795368..4846466hg38UCSC Ensembl
Outerchr11:4794868..4846966hg38UCSC Ensembl
chr11:4816598..4867696hg19UCSC Ensembl
Innerchr11:4816598..4867696hg19UCSC Ensembl
Outerchr11:4816098..4868196hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3851099
hg1951099
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625194
Supporting Variants
SamplesNA20807
Known GenesOR51F2, OR52R1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13999297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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