A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4427n100



Internal ID22790514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36103179..36252203hg38UCSC Ensembl
chr21:37475477..37624501hg19UCSC Ensembl
chr21:36397347..36546371hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38149025
hg19149025
hg18149025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066948, nsv1057101, nsv1061445, nsv1064839, nsv1063850, nsv1066727, nsv1056542, nsv1067039, nsv1057683, nsv1056304, nsv1059838, nsv1055706, nsv1063008, nsv1065905, nsv1067070, nsv1057827, nsv1067215
Samples
Known GenesCBR3, CBR3-AS1, DOPEY2, LOC100133286
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4427n100
Frequency
Sample Size11257
Observed Gain38
Observed Loss0
Observed Complex0
Frequencyn/a


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