A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3359



Internal ID15201274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34531574..34576232hg38UCSC Ensembl
Outerchr20:33119378..33164036hg19UCSC Ensembl
Outerchr20:32583039..32627697hg18UCSC Ensembl
Outerchr20:32583039..32627697hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3844659
hg1944659
hg1844659
hg1744659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7675
SamplesNA12156
Known GenesDYNLRB1, MAP1LC3A, PIGU
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv3359
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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