A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14033465



Internal ID2404900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14429513..14442828hg38UCSC Ensembl
Innerchr11:14429518..14442823hg38UCSC Ensembl
Outerchr11:14429508..14442833hg38UCSC Ensembl
chr11:14451059..14464374hg19UCSC Ensembl
Innerchr11:14451064..14464369hg19UCSC Ensembl
Outerchr11:14451054..14464379hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3813316
hg1913316
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625421
Supporting Variants
SamplesHG02133
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14033465
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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