A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487714



Internal ID265046
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 StatusM
Merged Variants
Supporting Variantsnssv17026353
Samples
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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