A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050544



Internal ID21959777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35733089..35834677hg38UCSC Ensembl
chr21:37105387..37206975hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38101589
hg19101589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050544
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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