A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589963



Internal ID16377372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26004870..26132290hg38UCSC Ensembl
Innerchr3:26046361..26173781hg19UCSC Ensembl
Innerchr3:26021365..26148785hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38127421
hg19127421
hg18127421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8265n54
Supporting Variantsnssv960139
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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