A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517718



Internal ID18815999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134478027..134869379hg38UCSC Ensembl
Innerchr11:134347921..134739273hg19UCSC Ensembl
Innerchr11:133853131..134244483hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38391353
hg19391353
hg18391353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046061
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)nssv3517718
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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