A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413191



Internal ID192486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94262016..94262067hg38UCSC Ensembl
chr9:97024298..97024349hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025748
Samples
Known GenesZNF169
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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