A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041551



Internal ID21950884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41806495..41806659hg38UCSC Ensembl
chr21:43226655..43226819hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644760
Samples
Known GenesPRDM15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041551
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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