A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433981



Internal ID212674
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 StatusM
Merged Variants
Supporting Variantsnssv16922920
Samples
Known GenesCYP20A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433981
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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