A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050961



Internal ID18793492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102123149..102382986hg38UCSC Ensembl
Innerchr11:101993880..102253717hg19UCSC Ensembl
Innerchr11:101499090..101758927hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38259838
hg19259838
hg18259838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1269n100
Supporting Variantsnssv3518886
Samples
Known GenesBIRC2, BIRC3, YAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050961
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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