A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850352



Internal ID22033995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3261772..3261772hg38UCSC Ensembl
chr20:3242418..3242418hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251182
Supporting Variants
Samples
Known GenesC20orf194
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850352
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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