A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844237



Internal ID22027880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234913361..234913361hg38UCSC Ensembl
chr1:235049108..235049108hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844237
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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