A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14037359



Internal ID2347974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16947328..16980505hg38UCSC Ensembl
chr11:16968875..17002052hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3833178
hg1933178
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625462
Supporting Variants
SamplesHG02084
Known GenesPLEKHA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14037359
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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