A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843606



Internal ID22027249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13837652..13837652hg38UCSC Ensembl
chr12:13990586..13990586hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240686
Supporting Variants
Samples
Known GenesGRIN2B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843606
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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