A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639493



Internal ID7026273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86851793..86862631hg38UCSC Ensembl
chr16:86885399..86896237hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3810839
hg1910839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15553967
SamplesHG03875
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639493
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