A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639567



Internal ID6679658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89089094..89123487hg38UCSC Ensembl
chr16:89155502..89189895hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3834394
hg1934394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv554e214
Supporting Variantsessv15567785, essv15567784
SamplesNA18555, HG04134
Known GenesACSF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639567
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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