A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591066



Internal ID16378475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98673640..98694015hg38UCSC Ensembl
Innerchr3:98392484..98412859hg19UCSC Ensembl
Innerchr3:99875174..99895549hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3820376
hg1920376
hg1820376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8459n54
Supporting Variantsnssv968219
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591066
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