A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536662



Internal ID312107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38434559..38436210hg38UCSC Ensembl
chr21:39806481..39808133hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381652
hg191653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726833
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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