A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453888



Internal ID18275198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10440315..10764692hg38UCSC Ensembl
Innerchr21:10747765..11072142hg19UCSC Ensembl
Innerchr21:9769636..10094013hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38324378
hg19324378
hg18324378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428382
Supporting Variants
SamplesNA19225
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
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)nssv453888
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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