A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003667



Internal ID19092885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82992228..83154255hg38UCSC Ensembl
Innerchr3:83041379..83203406hg19UCSC Ensembl
Innerchr3:83124069..83286096hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38162028
hg19162028
hg18162028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596245, nssv3596246
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)nsv1003667
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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