A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586442



Internal ID16373851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61715436..61742162hg38UCSC Ensembl
Innerchr20:60290492..60317218hg19UCSC Ensembl
Innerchr20:59723887..59750613hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3826727
hg1926727
hg1826727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7642n54
Supporting Variantsnssv1151406
SamplesHGDP00341
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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