A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850732



Internal ID22034375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33151865..33151865hg38UCSC Ensembl
chr21:34524171..34524171hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850732
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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