A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855911



Internal ID22039554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84462136..84462136hg38UCSC Ensembl
chr1:84927819..84927819hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855911
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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