A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151205



Internal ID15528360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14209133..14336744hg38UCSC Ensembl
Innerchr20:14189779..14317390hg19UCSC Ensembl
Innerchr20:14137779..14265390hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38127612
hg19127612
hg18127612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585439
Supporting Variants
SamplesHGDP00627
Known GenesFLRT3, MACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151205
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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