A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841555



Internal ID22025198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122917562..122917562hg38UCSC Ensembl
chr9:125679841..125679841hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841555
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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