A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3052n100



Internal ID19013420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82954267..83022527hg38UCSC Ensembl
chr16:82987872..83056132hg19UCSC Ensembl
chr16:81545373..81613633hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3868261
hg1968261
hg1868261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056005, nsv1064172, nsv1055246
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3052n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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