A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196363



Internal ID22346388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15181086..15186025hg38UCSC Ensembl
chr4:15182710..15187649hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg384940
hg194940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312306
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196363
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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