A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7619n54



Internal ID20141043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57525185..57526860hg38UCSC Ensembl
chr20:56100241..56101916hg19UCSC Ensembl
chr20:55533647..55535322hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381676
hg191676
hg181676
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586316, nsv586334, nsv586323, nsv586329, nsv586322, nsv586324
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7619n54
Frequency
Sample Size17421
Observed Gain23
Observed Loss23
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer