A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543526



Internal ID317768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99934255..99934290hg38UCSC Ensembl
chr9:102696537..102696572hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025536
Samples
Known GenesSTX17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543526
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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