A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486636



Internal ID263997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97038355..97038571hg38UCSC Ensembl
chr9:99800637..99800853hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027525
Samples
Known GenesCTSV
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486636
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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