A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586317



Internal ID16027040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57525185..57526860hg38UCSC Ensembl
Innerchr20:56100241..56101916hg19UCSC Ensembl
Innerchr20:55533647..55535322hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381676
hg191676
hg181676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7620n54
Supporting Variantsnssv941624, nssv941625, nssv941623
Samples
Known GenesCTCFL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586317
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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