A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589969



Internal ID16377378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26381978..26397467hg38UCSC Ensembl
Innerchr3:26423469..26438958hg19UCSC Ensembl
Innerchr3:26398473..26413962hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3815490
hg1915490
hg1815490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8266n54
Supporting Variantsnssv960147
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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