A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016108



Internal ID22077739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175864594..175927691hg38UCSC Ensembl
Outerchr3:175861809..175928368hg38UCSC Ensembl
Innerchr3:175582382..175645479hg19UCSC Ensembl
Outerchr3:175579597..175646156hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3866560
hg1966560
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156053
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016108
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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