A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589965



Internal ID16377374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26004870..26134292hg38UCSC Ensembl
Innerchr3:26046361..26175783hg19UCSC Ensembl
Innerchr3:26021365..26150787hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38129423
hg19129423
hg18129423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8265n54
Supporting Variantsnssv960141
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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