A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586422



Internal ID16027145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252260..61253113hg38UCSC Ensembl
Innerchr20:59827316..59828169hg19UCSC Ensembl
Innerchr20:59260711..59261564hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38854
hg19854
hg18854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7636n54
Supporting Variantsnssv941938, nssv941939, nssv941940, nssv941941
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586422
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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