A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840766



Internal ID22024409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14753870..14753870hg38UCSC Ensembl
chr9:14753868..14753868hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246898
Supporting Variants
Samples
Known GenesFREM1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840766
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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