A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772135



Internal ID18961046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24115197..24115402hg38UCSC Ensembl
chr16:24126518..24126723hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070761
Supporting Variants
SamplesKWP1
Known GenesPRKCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772135
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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