A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590606



Internal ID16031329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71752561..71754736hg38UCSC Ensembl
Innerchr3:71801712..71803887hg19UCSC Ensembl
Innerchr3:71884402..71886577hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382176
hg192176
hg182176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965549
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590606
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