A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589786



Internal ID16377195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15802839..15804559hg38UCSC Ensembl
Innerchr3:15844346..15846066hg19UCSC Ensembl
Innerchr3:15819350..15821070hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381721
hg191721
hg181721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8237n54
Supporting Variantsnssv959457
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589786
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