A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011564



Internal ID22073195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15147437..15322653hg38UCSC Ensembl
Outerchr16:15100205..15388077hg38UCSC Ensembl
Innerchr16:15241294..15416510hg19UCSC Ensembl
Outerchr16:15194062..15481934hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38287873
hg19287873
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155246
Supporting Variants
Samples
Known GenesMIR3180-4, MIR6511B-1, NPIPA5, PDXDC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011564
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