A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1053n54



Internal ID22768948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38576045..38729937hg38UCSC Ensembl
chr10:38869176..39023068hg19UCSC Ensembl
chr10:38909182..39063074hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38153893
hg19153893
hg18153893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550476, nsv550491, nsv550496, nsv550475
Samples
Known GenesACTR3BP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1053n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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