A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001930



Internal ID19091147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165272478..165462957hg38UCSC Ensembl
Innerchr3:164990266..165180745hg19UCSC Ensembl
Innerchr3:166472960..166663439hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38190480
hg19190480
hg18190480
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738254
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)nsv1001930
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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