A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586404



Internal ID16027127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252058..61253113hg38UCSC Ensembl
Innerchr20:59827114..59828169hg19UCSC Ensembl
Innerchr20:59260509..59261564hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381056
hg191056
hg181056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7636n54
Supporting Variantsnssv941879, nssv941878
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586404
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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