A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589883



Internal ID16377292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21131649..21248563hg38UCSC Ensembl
Innerchr3:21173141..21290055hg19UCSC Ensembl
Innerchr3:21148145..21265059hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38116915
hg19116915
hg18116915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959906
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589883
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