A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840827



Internal ID22024470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21857026..21857026hg38UCSC Ensembl
chr9:21857025..21857025hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246959
Supporting Variants
Samples
Known GenesMTAP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840827
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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