A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155274



Internal ID22085779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21503753..21575403hg38UCSC Ensembl
Outerchr16:21401082..21577467hg38UCSC Ensembl
Innerchr16:21515074..21586724hg19UCSC Ensembl
Outerchr16:21412403..21588788hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38176386
hg19176386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv110n97
Supporting Variantsnssv4011606
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155274
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