A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589884



Internal ID16377293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21199656..21316760hg38UCSC Ensembl
Innerchr3:21241148..21358252hg19UCSC Ensembl
Innerchr3:21216152..21333256hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38117105
hg19117105
hg18117105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8256n54
Supporting Variantsnssv959907
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589884
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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