A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4468n100



Internal ID20156084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18760915..19019471hg38UCSC Ensembl
chr22:18748428..19006984hg19UCSC Ensembl
chr22:17128428..17386984hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38258557
hg19258557
hg18258557
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057148, nsv1058703, nsv1062299, nsv1058215
Samples
Known GenesDGCR5, DGCR6, DGCR9, GGT3P, PRODH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4468n100
Frequency
Sample Size29084
Observed Gain57
Observed Loss9
Observed Complex0
Frequencyn/a


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