A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844239



Internal ID22027882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235002709..235002709hg38UCSC Ensembl
chr1:235138456..235138456hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844239
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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