A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638265



Internal ID7025051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25056562..25087102hg38UCSC Ensembl
chr16:25067883..25098423hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3830541
hg1930541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15431180
SamplesNA19209
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638265
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer