A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5545370



Internal ID319418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102633367..102633406hg38UCSC Ensembl
chr14:103099704..103099743hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698380
Samples
Known GenesRCOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5545370
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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