A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514809



Internal ID18813090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119899472..119918974hg38UCSC Ensembl
Innerchr11:119770181..119789683hg19UCSC Ensembl
Innerchr11:119275391..119294893hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3819503
hg1919503
hg1819503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051760
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)nssv3514809
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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