A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2977n100



Internal ID20154593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50744296..50798809hg38UCSC Ensembl
chr16:50778207..50832720hg19UCSC Ensembl
chr16:49335708..49390221hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3854514
hg1954514
hg1854514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058852, nsv1064235, nsv1067006
Samples
Known GenesCYLD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2977n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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