A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453753



Internal ID18621870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35638900..35894515hg38UCSC Ensembl
Innerchr2:35863966..36119581hg19UCSC Ensembl
Innerchr2:35717470..35973085hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38255616
hg19255616
hg18255616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428390
Supporting Variants
SamplesNA19189
Known Genes
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)nssv453753
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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