A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586433



Internal ID16373842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61397832..61416793hg38UCSC Ensembl
Innerchr20:59972888..59991849hg19UCSC Ensembl
Innerchr20:59406283..59425244hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818962
hg1918962
hg1818962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151399
SamplesHGDP00251
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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