A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638561



Internal ID6678658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47463995..47559918hg38UCSC Ensembl
chr16:47497906..47593829hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3895924
hg1995924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15472435
SamplesNA18967
Known GenesPHKB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638561
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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