A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4385n100



Internal ID20156001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:13363977..14135181hg38UCSC Ensembl
chr21:14736298..15507502hg19UCSC Ensembl
chr21:13658169..14429373hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38771205
hg19771205
hg18771205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055396, nsv1062639, nsv1067433
Samples
Known GenesANKRD20A11P, C21orf15, LIPI, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4385n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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