A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453898



Internal ID18273419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10337224..10510486hg38UCSC Ensembl
Innerchr21:11001971..11175233hg19UCSC Ensembl
Innerchr21:10023842..10197104hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38173263
hg19173263
hg18173263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428382
Supporting Variants
SamplesHGDP00467
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
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)nssv453898
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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