A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638900



Internal ID7025685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68008886..68035332hg38UCSC Ensembl
chr16:68042789..68069235hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3826447
hg1926447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501612
SamplesHG02976
Known GenesDDX28, DUS2, LOC100131303
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638900
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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