A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852864



Internal ID22036507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186597288..186597288hg38UCSC Ensembl
chr3:186315077..186315077hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852864
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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