A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156022



Internal ID22086527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143050037..143076956hg38UCSC Ensembl
Outerchr3:143046124..143081405hg38UCSC Ensembl
Innerchr3:142768879..142795798hg19UCSC Ensembl
Outerchr3:142764966..142800247hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3835282
hg1935282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015898
Samples
Known GenesU2SURP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156022
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