A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504274



Internal ID18455869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134322594..134625980hg38UCSC Ensembl
Innerchr11:134192488..134495874hg19UCSC Ensembl
Innerchr11:133697698..134001084hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38303387
hg19303387
hg18303387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037759
Supporting Variants
Samples
Known GenesB3GAT1, GLB1L2, LOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504274
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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