A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066350



Internal ID19155569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21778036..21811958hg38UCSC Ensembl
Innerchr20:21758674..21792596hg19UCSC Ensembl
Innerchr20:21706674..21740596hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3833923
hg1933923
hg1833923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584651
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066350
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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