A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732212



Internal ID155878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36663047..36663098hg38UCSC Ensembl
chr20:35291450..35291501hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429341
Supporting Variants
Samples
Known GenesNDRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732212
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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