A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541664



Internal ID316239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41560313..41560639hg38UCSC Ensembl
chr21:42932240..42932566hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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