A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15439009



Internal ID4110566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26849448..26863424hg38UCSC Ensembl
chr16:26860769..26874745hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3813977
hg1913977
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638307
Supporting Variants
SamplesHG03731
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15439009
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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