A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532933



Internal ID308837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24476190..24477001hg38UCSC Ensembl
chr20:24456826..24457637hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731689
Samples
Known GenesSYNDIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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