A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489451



Internal ID266731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98071724..98109618hg38UCSC Ensembl
chr9:100834006..100871900hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3837895
hg1937895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026872
Samples
Known GenesNANS, TRIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489451
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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