A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502379



Internal ID279247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102354711..102354994hg38UCSC Ensembl
chr14:102821048..102821331hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698349
Samples
Known GenesCINP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502379
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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