A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062312



Internal ID19151531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4040286..4070778hg38UCSC Ensembl
Innerchr20:4020933..4051425hg19UCSC Ensembl
Innerchr20:3968933..3999425hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3830493
hg1930493
hg1830493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734865
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)nsv1062312
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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