A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501529



Internal ID278425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35233089..35233672hg38UCSC Ensembl
chr14:35702295..35702878hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695542
Samples
Known GenesKIAA0391
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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