A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518306



Internal ID18816587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101796427..101849337hg38UCSC Ensembl
Innerchr11:101667158..101720068hg19UCSC Ensembl
Innerchr11:101172368..101225278hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3852911
hg1952911
hg1852911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048625
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)nssv3518306
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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