A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026353



Internal ID85311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113089900..113122600hg38UCSC Ensembl
chr9:115852180..115884880hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3832701
hg1932701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487714
Supporting Variants
Samples
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026353
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001254


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