A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15530806



Internal ID3501362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79159212..79163978hg38UCSC Ensembl
chr16:79193109..79197875hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg384767
hg194767
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639239
Supporting Variants
SamplesHG03108
Known GenesWWOX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15530806
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