A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090149



Internal ID4275620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35086229..35097448hg38UCSC Ensembl
Innerchr11:35086231..35097446hg38UCSC Ensembl
Outerchr11:35086227..35097450hg38UCSC Ensembl
chr11:35107776..35118995hg19UCSC Ensembl
Innerchr11:35107778..35118993hg19UCSC Ensembl
Outerchr11:35107774..35118997hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811220
hg1911220
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625920
Supporting Variants
SamplesHG03838
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090149
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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