A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5461n100



Internal ID22791548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166234573..166273816hg38UCSC Ensembl
chr4:167155725..167194968hg19UCSC Ensembl
chr4:167375175..167414418hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3839244
hg1939244
hg1839244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028616, nsv1034110
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5461n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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