A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589569



Internal ID16030292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6825831..6866848hg38UCSC Ensembl
Innerchr3:6867518..6908535hg19UCSC Ensembl
Innerchr3:6842518..6883535hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3841018
hg1941018
hg1841018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958603
Samples
Known GenesGRM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589569
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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