A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006665



Internal ID19095882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89909694..90113043hg38UCSC Ensembl
Innerchr3:89958844..90162193hg19UCSC Ensembl
Innerchr3:90041534..90244883hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38203350
hg19203350
hg18203350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4811n100
Supporting Variantsnssv3603281
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)nsv1006665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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