A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027093



Internal ID85783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109027239..109027239hg38UCSC Ensembl
chr9:111789519..111789519hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546614
Supporting Variants
Samples
Known GenesTMEM245
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027093
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003445


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