A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453583



Internal ID18621413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25452781..25628359hg38UCSC Ensembl
Innerchr18:23032745..23208323hg19UCSC Ensembl
Innerchr18:21286743..21462321hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38175579
hg19175579
hg18175579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428354
Supporting Variants
SamplesNA19096
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)nssv453583
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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