A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286331



Internal ID22117991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33176922..33181586hg38UCSC Ensembl
chr19:33667828..33672492hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384665
hg194665
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211129
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286331
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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