A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485316



Internal ID262708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92250615..92250677hg38UCSC Ensembl
chr9:95012897..95012959hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027404
Samples
Known GenesIARS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485316
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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