A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4510n100



Internal ID22790597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22427263..22604355hg38UCSC Ensembl
chr22:22781599..22946825hg19UCSC Ensembl
chr22:21111599..21276825hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38177093
hg19165227
hg18165227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056678, nsv1056468
Samples
Known GenesLOC648691, PRAME, ZNF280A, ZNF280B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4510n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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