A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589890



Internal ID16377299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21217702..21292515hg38UCSC Ensembl
Innerchr3:21259194..21334007hg19UCSC Ensembl
Innerchr3:21234198..21309011hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3874814
hg1974814
hg1874814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8257n54
Supporting Variantsnssv959916
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589890
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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