A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14216191



Internal ID3405334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80257345..80275559hg38UCSC Ensembl
Innerchr11:80257845..80275059hg38UCSC Ensembl
Outerchr11:80256345..80276559hg38UCSC Ensembl
chr11:79968389..79986603hg19UCSC Ensembl
Innerchr11:79968889..79986103hg19UCSC Ensembl
Outerchr11:79967389..79987603hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3818215
hg1918215
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626930
Supporting Variants
SamplesHG03052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14216191
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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