A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516274



Internal ID18814555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5864481..5914268hg38UCSC Ensembl
Innerchr11:5885711..5935498hg19UCSC Ensembl
Innerchr11:5842287..5892074hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3849788
hg1949788
hg1849788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041535
Supporting Variants
Samples
Known GenesOR52E4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516274
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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