A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641321



Internal ID21833368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28918362..28919188hg38UCSC Ensembl
chr21:30290684..30291510hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641321
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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