A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586436



Internal ID16373845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61639511..61713822hg38UCSC Ensembl
Innerchr20:60214567..60288878hg19UCSC Ensembl
Innerchr20:59647962..59722273hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3874312
hg1974312
hg1874312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151400
SamplesHGDP00388
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586436
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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