A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050907



Internal ID21960141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32686800..32693382hg38UCSC Ensembl
chr21:34059110..34065692hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg386583
hg196583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648755
Samples
Known GenesSYNJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050907
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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