A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14113206



Internal ID4115022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43480613..43496244hg38UCSC Ensembl
chr11:43502163..43517794hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3815632
hg1915632
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626146
Supporting Variants
SamplesNA21102
Known GenesTTC17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14113206
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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