A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453201



Internal ID18273897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33723154..34005293hg38UCSC Ensembl
Innerchr16:33525621..33807760hg19UCSC Ensembl
Innerchr16:33433122..33715261hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38282140
hg19282140
hg18282140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428325
Supporting Variants
SamplesHGDP00984
Known GenesRNU6-76P
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)nssv453201
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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