A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641382



Internal ID21833429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8231387..8231461hg38UCSC Ensembl
chrUn_gl000220:129983..130073hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3875
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641382
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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