A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639611



Internal ID7026390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90072245..90098346hg38UCSC Ensembl
chr16:90138653..90164754hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3826102
hg1926102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15570148
SamplesNA18933
Known GenesPRDM7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639611
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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