A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155245



Internal ID22085750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15147437..15312570hg38UCSC Ensembl
Outerchr16:15100205..15322653hg38UCSC Ensembl
Innerchr16:15241294..15406427hg19UCSC Ensembl
Outerchr16:15194062..15416510hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38222449
hg19222449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n97
Supporting Variantsnssv4011563
Samples
Known GenesMIR3180-4, MIR6511B-1, PDXDC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155245
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