A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156041



Internal ID22086546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163877778..164177912hg38UCSC Ensembl
Outerchr3:163874417..164188095hg38UCSC Ensembl
Innerchr3:163595566..163895700hg19UCSC Ensembl
Outerchr3:163592205..163905883hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38313679
hg19313679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016094
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156041
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