A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150639



Internal ID18850994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:23899619..23899885hg38UCSC Ensembl
Outerchr16:23910940..23911206hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996113
SamplesKWB1
Known GenesPRKCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150639
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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