A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590216



Internal ID16030939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47449222..47451772hg38UCSC Ensembl
Innerchr3:47490712..47493262hg19UCSC Ensembl
Innerchr3:47465716..47468266hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382551
hg192551
hg182551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8312n54
Supporting Variantsnssv962615, nssv962616
Samples
Known GenesSCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590216
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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