A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4565n100



Internal ID22790652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37374317..37422295hg38UCSC Ensembl
chr22:37770357..37818333hg19UCSC Ensembl
chr22:36100303..36148279hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3847979
hg1947977
hg1847977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060216, nsv1062363, nsv1061788
Samples
Known GenesELFN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4565n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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