A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428162



Internal ID18624612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11046157..11319706hg38UCSC Ensembl
Innerchr7:11085784..11359333hg19UCSC Ensembl
Innerchr7:11052309..11325858hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38273550
hg19273550
hg18273550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450921
SamplesHGDP00449
Known GenesPHF14
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)nsv428162
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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