A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590154



Internal ID16377563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:43286381..43292528hg38UCSC Ensembl
Innerchr3:43327873..43334020hg19UCSC Ensembl
Innerchr3:43302877..43309024hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386148
hg196148
hg186148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8300n54
Supporting Variantsnssv962440
Samples
Known GenesSNRK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590154
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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