A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4457n100



Internal ID22790544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:16384224..16550182hg38UCSC Ensembl
chr22:16864886..17031072hg19UCSC Ensembl
chr22:15244886..15411072hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38165959
hg19166187
hg18166187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058625, nsv1066902
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)dgv4457n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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