A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591922



Internal ID16379331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143926400..144106597hg38UCSC Ensembl
Innerchr3:143645242..143825439hg19UCSC Ensembl
Innerchr3:145127932..145308129hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38180198
hg19180198
hg18180198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975221
Samples
Known GenesC3orf58
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer