A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955361



Internal ID17304234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:142017759..142028258hg38UCSC Ensembl
Outerchr3:141736601..141747100hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001478
SamplesBILGI_BIOE
Known GenesTFDP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955361
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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