A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14100709



Internal ID5703097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39695146..39697469hg38UCSC Ensembl
Innerchr11:39695146..39697469hg38UCSC Ensembl
Outerchr11:39694933..39697653hg38UCSC Ensembl
chr11:39716696..39719019hg19UCSC Ensembl
Innerchr11:39716696..39719019hg19UCSC Ensembl
Outerchr11:39716483..39719203hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382324
hg192324
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626047
Supporting Variants
SamplesNA19090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14100709
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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