A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550445



Internal ID323999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38435894..38436001hg38UCSC Ensembl
chr21:39807817..39807924hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726834
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550445
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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