A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512690



Internal ID18810971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116382452..116415213hg38UCSC Ensembl
Innerchr11:116253169..116285930hg19UCSC Ensembl
Innerchr11:115758379..115791140hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832762
hg1932762
hg1832762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044015
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)nssv3512690
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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