A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001498



Internal ID16947764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:172513711..172523610hg38UCSC Ensembl
Outerchr3:172231501..172241400hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954508
Supporting Variants
SamplesBILGI_BIOE
Known GenesTNFSF10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001498
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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