A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220105



Internal ID22364908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102740322..102745017hg38UCSC Ensembl
chr14:103206659..103211354hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384696
hg194696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375510
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220105
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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