A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520489



Internal ID18818770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32425801..32443687hg38UCSC Ensembl
Innerchr11:32447347..32465233hg19UCSC Ensembl
Innerchr11:32403923..32421809hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3817887
hg1917887
hg1817887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051559
Supporting Variants
Samples
Known GenesWT1, WT1-AS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520489
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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