A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647639



Internal ID21839686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36058410..36059261hg38UCSC Ensembl
chr21:37430708..37431559hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054854
Supporting Variants
Samples
Known GenesSETD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647639
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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