A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002152



Internal ID18744683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41228025..41246202hg38UCSC Ensembl
Innerchr3:41269516..41287693hg19UCSC Ensembl
Innerchr3:41244520..41262697hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3818178
hg1918178
hg1818178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589704
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)nsv1002152
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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