A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003473



Internal ID19092691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11895928..11919376hg38UCSC Ensembl
Innerchr3:11937402..11960850hg19UCSC Ensembl
Innerchr3:11912402..11935850hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3823449
hg1923449
hg1823449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4685n100
Supporting Variantsnssv3591965
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)nsv1003473
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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