A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507437



Internal ID284156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100478041..100480968hg38UCSC Ensembl
chr14:100944378..100947305hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698801
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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