A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591158



Internal ID16031881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100626357..100691880hg38UCSC Ensembl
Innerchr3:100345201..100410724hg19UCSC Ensembl
Innerchr3:101827891..101893414hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3865524
hg1965524
hg1865524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8477n54
Supporting Variantsnssv970690
Samples
Known GenesGPR128
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591158
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