A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155958



Internal ID22086463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34464158..34504111hg38UCSC Ensembl
Outerchr3:34457792..34504909hg38UCSC Ensembl
Innerchr3:34505650..34545603hg19UCSC Ensembl
Outerchr3:34499284..34546401hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3847118
hg1947118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016338
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155958
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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