A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065081



Internal ID19154300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18901576..18914058hg38UCSC Ensembl
Innerchr20:18882220..18894702hg19UCSC Ensembl
Innerchr20:18830220..18842702hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3812483
hg1912483
hg1812483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584645
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)nsv1065081
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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