A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591619



Internal ID16379028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128664254..128694054hg38UCSC Ensembl
Innerchr3:128383097..128412897hg19UCSC Ensembl
Innerchr3:129865787..129895587hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3829801
hg1929801
hg1829801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8569n54
Supporting Variantsnssv973024
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591619
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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