A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710076



Internal ID19008357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33361539..33481756hg38UCSC Ensembl
Innerchr11:33383085..33503302hg19UCSC Ensembl
Innerchr11:33339661..33459878hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38120218
hg19120218
hg18120218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037452
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710076
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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