A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5852n54



Internal ID22773747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9913909..9914947hg38UCSC Ensembl
chr18:9913906..9914944hg19UCSC Ensembl
chr18:9903906..9904944hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381039
hg191039
hg181039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576458, nsv576460, nsv576461, nsv576469, nsv576466, nsv576467, nsv576459
Samples
Known GenesVAPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5852n54
Frequency
Sample Size17421
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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