A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692551



Internal ID116217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98841764..98841925hg38UCSC Ensembl
chr13:99494018..99494179hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506673
Supporting Variants
Samples
Known GenesDOCK9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692551
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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