A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590975



Internal ID16378384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90259908..90403492hg38UCSC Ensembl
Innerchr3:90309058..90452642hg19UCSC Ensembl
Innerchr3:90391748..90535332hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38143585
hg19143585
hg18143585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8441n54
Supporting Variantsnssv967760
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590975
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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