A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4962n54



Internal ID20138386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27320573..27339707hg38UCSC Ensembl
chr16:27331894..27351028hg19UCSC Ensembl
chr16:27239395..27258529hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3819135
hg1919135
hg1819135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571714, nsv571713
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4962n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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