A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046769



Internal ID18789300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76158693..76253330hg38UCSC Ensembl
Innerchr11:75869737..75964374hg19UCSC Ensembl
Innerchr11:75547385..75642022hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3894638
hg1994638
hg1894638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1227n100
Supporting Variantsnssv3507995, nssv3510974
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)nsv1046769
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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