A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555131



Internal ID5556947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87320763..87352951hg38UCSC Ensembl
chr16:87354369..87386557hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3832189
hg1932189
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639511
Supporting Variants
SamplesNA12272
Known GenesFBXO31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555131
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