A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590192



Internal ID16030915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46755299..46802757hg38UCSC Ensembl
Innerchr3:46796789..46844247hg19UCSC Ensembl
Innerchr3:46771793..46819251hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3847459
hg1947459
hg1847459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8304n54
Supporting Variantsnssv962569
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590192
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