A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852899



Internal ID22036542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189148835..189148835hg38UCSC Ensembl
chr3:188866624..188866624hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260141
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852899
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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