A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850745



Internal ID22034388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35551524..35551524hg38UCSC Ensembl
chr21:36923822..36923822hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251869
Supporting Variants
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850745
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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