A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14309558



Internal ID22138831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141442513..141443606hg38UCSC Ensembl
chr3:141161355..141162448hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200306
Supporting Variants
SamplesHG00513
Known GenesZBTB38
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14309558
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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