A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940963



Internal ID15888233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47733014..47885094hg38UCSC Ensembl
Innerchr20:46361758..46513838hg19UCSC Ensembl
Innerchr20:45795165..45947245hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38152081
hg19152081
hg18152081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586156
Supporting Variants
Samples
Known GenesSULF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940963
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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