A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591633



Internal ID16379042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128680780..128691442hg38UCSC Ensembl
Innerchr3:128399623..128410285hg19UCSC Ensembl
Innerchr3:129882313..129892975hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3810663
hg1910663
hg1810663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8573n54
Supporting Variantsnssv973046
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591633
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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