A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453157



Internal ID18274733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32803560..32983269hg38UCSC Ensembl
Innerchr16:32814881..32994590hg19UCSC Ensembl
Innerchr16:32722382..32902091hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38179710
hg19179710
hg18179710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428325
Supporting Variants
SamplesNA19108
Known GenesSLC6A10P
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)nssv453157
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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