A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5203n100



Internal ID22791290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48168652..48184712hg38UCSC Ensembl
chr4:48170669..48186729hg19UCSC Ensembl
chr4:47865426..47881486hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3816061
hg1916061
hg1816061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011820, nsv1011366, nsv1005668
Samples
Known GenesTEC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5203n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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