A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513441



Internal ID18811722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134478027..134849662hg38UCSC Ensembl
Innerchr11:134347921..134719556hg19UCSC Ensembl
Innerchr11:133853131..134224766hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38371636
hg19371636
hg18371636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036716
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513441
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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