A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569847



Internal ID5571663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89680115..89694466hg38UCSC Ensembl
chr16:89746523..89760874hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3814352
hg1914352
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639592
Supporting Variants
SamplesNA20818
Known GenesCDK10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569847
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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