A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040591



Internal ID18783122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76161714..76196288hg38UCSC Ensembl
Innerchr11:75872758..75907332hg19UCSC Ensembl
Innerchr11:75550406..75584980hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3834575
hg1934575
hg1834575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1226n100
Supporting Variantsnssv3507795
Samples
Known GenesWNT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040591
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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