A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453961



Internal ID18275314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18069029..18780583hg38UCSC Ensembl
Innerchr22:18551795..18768096hg19UCSC Ensembl
Innerchr22:16931795..17148096hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38711555
hg19216302
hg18216302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428385
Supporting Variants
SamplesNA19257
Known GenesGGT3P, PEX26, TUBA8, USP18
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)nssv453961
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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