A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070760



Internal ID18971778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24049371..24049580hg38UCSC Ensembl
chr16:24060692..24060901hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767454
SamplesKWP1
Known GenesPRKCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070760
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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