A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151521



Internal ID19196856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65690396..65695697hg38UCSC Ensembl
Outerchr16:65724299..65729600hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002942
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151521
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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