A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4561n100



Internal ID22790648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32610981..32705152hg38UCSC Ensembl
chr22:33006967..33101138hg19UCSC Ensembl
chr22:31336967..31431138hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3894172
hg1994172
hg1894172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061824, nsv1055541
Samples
Known GenesSYN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4561n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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