A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844099



Internal ID22027742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69728858..69728858hg38UCSC Ensembl
chr12:70122638..70122638hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844099
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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