A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586439



Internal ID16373848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61693013..61723194hg38UCSC Ensembl
Innerchr20:60268069..60298250hg19UCSC Ensembl
Innerchr20:59701464..59731645hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3830182
hg1930182
hg1830182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7641n54
Supporting Variantsnssv1151402
SamplesHGDP00033
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586439
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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