A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7623n54



Internal ID20141047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57525592..57527189hg38UCSC Ensembl
chr20:56100648..56102245hg19UCSC Ensembl
chr20:55534054..55535651hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381598
hg191598
hg181598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586343, nsv586339, nsv586341, nsv586342
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7623n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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