A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766150



Internal ID18963515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50245588..50246489hg38UCSC Ensembl
chr16:50279499..50280400hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069944
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766150
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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