A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428377



Internal ID18624827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61418449..61530272hg38UCSC Ensembl
Innerchr20:59993505..60105328hg19UCSC Ensembl
Innerchr20:59426900..59538723hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38111824
hg19111824
hg18111824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv453849
SamplesNA18498
Known GenesCDH4
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nsv428377
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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