A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052159



Internal ID18794690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101568924..101982562hg38UCSC Ensembl
Innerchr11:101439655..101853293hg19UCSC Ensembl
Innerchr11:100944865..101358503hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38413639
hg19413639
hg18413639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518986
Samples
Known GenesANGPTL5, KIAA1377, TRPC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052159
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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