A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5937n54



Internal ID22773832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52603967..52631750hg38UCSC Ensembl
chr18:50130337..50158120hg19UCSC Ensembl
chr18:48384335..48412118hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3827784
hg1927784
hg1827784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576931, nsv576933, nsv576934, nsv576932
Samples1780854206_A
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5937n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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