A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535015



Internal ID310732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32495031..32627711hg38UCSC Ensembl
chr21:33867341..34000021hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38132681
hg19132681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726605
Samples
Known GenesC21orf59, EVA1C, TCP10L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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