A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710793



Internal ID19009074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134867789..134960188hg38UCSC Ensembl
Innerchr11:134737683..134830082hg19UCSC Ensembl
Innerchr11:134242893..134335292hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3892400
hg1992400
hg1892400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050154
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)nssv3710793
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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