A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586410



Internal ID16027133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252123..61253059hg38UCSC Ensembl
Innerchr20:59827179..59828115hg19UCSC Ensembl
Innerchr20:59260574..59261510hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38937
hg19937
hg18937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7635n54
Supporting Variantsnssv941900
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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