A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453511



Internal ID18620653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52270800..52434176hg38UCSC Ensembl
Innerchr17:50348160..50511536hg19UCSC Ensembl
Innerchr17:47703159..47866535hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38163377
hg19163377
hg18163377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428345
Supporting Variants
SamplesHGDP00986
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)nssv453511
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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