A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638267



Internal ID6678365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25097954..25119835hg38UCSC Ensembl
chr16:25109275..25131156hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3821882
hg1921882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15431184, essv15431183
SamplesNA19209, HG03692
Known GenesLCMT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638267
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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