A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050426



Internal ID19139645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80375396..80437364hg38UCSC Ensembl
Innerchr11:80086440..80148408hg19UCSC Ensembl
Innerchr11:79764088..79826056hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3861969
hg1961969
hg1861969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520881
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)nsv1050426
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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