A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591038



Internal ID16378447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96813227..96814420hg38UCSC Ensembl
Innerchr3:96532071..96533264hg19UCSC Ensembl
Innerchr3:98014761..98015954hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv968103, nssv968102
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591038
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer