A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922920



Internal ID16038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203297784..203298692hg38UCSC Ensembl
chr2:204162507..204163415hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433981
Supporting Variants
Samples
Known GenesCYP20A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922920
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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