A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7618n54



Internal ID20141042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57525185..57526763hg38UCSC Ensembl
chr20:56100241..56101819hg19UCSC Ensembl
chr20:55533647..55535225hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381579
hg191579
hg181579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586314, nsv586315
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7618n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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