A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586418



Internal ID16027141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61252182..61253165hg38UCSC Ensembl
Innerchr20:59827238..59828221hg19UCSC Ensembl
Innerchr20:59260633..59261616hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38984
hg19984
hg18984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7636n54
Supporting Variantsnssv941923, nssv941924, nssv941922, nssv941920, nssv941925, nssv941926, nssv941921
Samples
Known GenesCDH4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586418
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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