A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849971



Internal ID22033614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38018628..38018628hg38UCSC Ensembl
chr20:36647030..36647030hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251425
Supporting Variants
Samples
Known GenesTTI1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849971
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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