A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051187



Internal ID19140406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15759731..15824990hg38UCSC Ensembl
Innerchr11:15781277..15846536hg19UCSC Ensembl
Innerchr11:15737853..15803112hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3865260
hg1965260
hg1865260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513650
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)nsv1051187
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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