A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842007



Internal ID22025650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129560574..129560574hg38UCSC Ensembl
chr9:132322853..132322853hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842007
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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