A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590970



Internal ID16378379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89938721..90392156hg38UCSC Ensembl
Innerchr3:89987871..90441306hg19UCSC Ensembl
Innerchr3:90070561..90523996hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38453436
hg19453436
hg18453436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967755
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590970
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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