A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5292n100



Internal ID19015660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68804789..68843354hg38UCSC Ensembl
chr4:69670507..69709072hg19UCSC Ensembl
chr4:69705096..69743661hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3838566
hg1938566
hg1838566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012268, nsv1003090, nsv1006812
Samples
Known GenesUGT2B10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5292n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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