A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841774



Internal ID22025417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104569354..104569354hg38UCSC Ensembl
chr9:107331635..107331635hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240083
Supporting Variants
Samples
Known GenesOR13C8
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841774
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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