A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051279



Internal ID19140498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84107604..84161772hg38UCSC Ensembl
Innerchr11:83818647..83872815hg19UCSC Ensembl
Innerchr11:83496295..83550463hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3854169
hg1954169
hg1854169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513705
Samples
Known GenesDLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051279
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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