A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840949



Internal ID22024592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21981138..21981138hg38UCSC Ensembl
chr9:21981137..21981137hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246961
Supporting Variants
Samples
Known GenesCDKN2A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840949
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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