A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768247



Internal ID15715517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11956026..11977482hg38UCSC Ensembl
Innerchr11:11977573..11999029hg19UCSC Ensembl
Innerchr11:11934149..11955605hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3821457
hg1921457
hg1821457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553544
Supporting Variants
Samples
Known GenesDKK3, USP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768247
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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