A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010088



Internal ID18752619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41227301..41238389hg38UCSC Ensembl
Innerchr3:41268792..41279880hg19UCSC Ensembl
Innerchr3:41243796..41254884hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3811089
hg1911089
hg1811089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589703
Samples
Known GenesCTNNB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010088
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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