A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14029873



Internal ID3689149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11754786..11760303hg38UCSC Ensembl
Innerchr11:11754786..11760303hg38UCSC Ensembl
Outerchr11:11754649..11760354hg38UCSC Ensembl
chr11:11776333..11781850hg19UCSC Ensembl
Innerchr11:11776333..11781850hg19UCSC Ensembl
Outerchr11:11776196..11781901hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385518
hg195518
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625378
Supporting Variants
SamplesHG03295
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14029873
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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