A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589894



Internal ID16377303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21217943..21328094hg38UCSC Ensembl
Innerchr3:21259435..21369586hg19UCSC Ensembl
Innerchr3:21234439..21344590hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38110152
hg19110152
hg18110152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8256n54
Supporting Variantsnssv959918
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589894
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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