A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059236



Internal ID18801767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53485342..53596991hg38UCSC Ensembl
Innerchr20:52101881..52213530hg19UCSC Ensembl
Innerchr20:51535288..51646937hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38111650
hg19111650
hg18111650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731367
Samples
Known GenesTSHZ2, ZNF217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059236
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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