A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586416



Internal ID16027139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252182..61252852hg38UCSC Ensembl
Innerchr20:59827238..59827908hg19UCSC Ensembl
Innerchr20:59260633..59261303hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38671
hg19671
hg18671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7634n54
Supporting Variantsnssv941916
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586416
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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