A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637585



Internal ID6677688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:798001..812299hg38UCSC Ensembl
chr16:848001..862299hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814299
hg1914299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355400
SamplesHG02805
Known GenesCHTF18, GNG13, PRR25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637585
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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