A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14295596



Internal ID4393197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121856727..121866001hg38UCSC Ensembl
chr11:121727435..121736709hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg389275
hg199275
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627931
Supporting Variants
SamplesHG03914
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14295596
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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