A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521534



Internal ID18473129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76160196..76286619hg38UCSC Ensembl
Innerchr11:75871240..75997663hg19UCSC Ensembl
Innerchr11:75548888..75675311hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38126424
hg19126424
hg18126424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053129
Supporting Variants
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)nssv3521534
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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