A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638850



Internal ID7025635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65331376..65387294hg38UCSC Ensembl
chr16:65365279..65421197hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3855919
hg1955919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15499466
SamplesHG01092
Known GenesLINC00922
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638850
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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