A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453852



Internal ID18275255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61886206..62008187hg38UCSC Ensembl
Innerchr20:60461262..60583243hg19UCSC Ensembl
Innerchr20:59894657..60016638hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38121982
hg19121982
hg18121982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428378
Supporting Variants
SamplesNA19225
Known GenesCDH4, MIR1257, TAF4
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)nssv453852
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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