A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011723



Internal ID22073354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21503753..21591309hg38UCSC Ensembl
Outerchr16:21401082..21594646hg38UCSC Ensembl
Innerchr16:21515074..21602630hg19UCSC Ensembl
Outerchr16:21412403..21605967hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38193565
hg19193565
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155279
Supporting Variants
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011723
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