A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487587



Internal ID264921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15218888..15221581hg38UCSC Ensembl
chr9:15218886..15221579hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382694
hg192694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020583
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487587
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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