A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591032



Internal ID16378441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95958848..96022412hg38UCSC Ensembl
Innerchr3:95677692..95741256hg19UCSC Ensembl
Innerchr3:97160382..97223946hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3863565
hg1963565
hg1863565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv968098
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591032
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