A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591381



Internal ID16378790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119633222..119634997hg38UCSC Ensembl
Innerchr3:119352069..119353844hg19UCSC Ensembl
Innerchr3:120834759..120836534hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381776
hg191776
hg181776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8520n54
Supporting Variantsnssv971735
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591381
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