A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539025



Internal ID314027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42008990..42009123hg38UCSC Ensembl
chr21:43429099..43429232hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727030
Samples
Known GenesZBTB21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539025
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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