A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048967



Internal ID21958201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16626681..16626753hg38UCSC Ensembl
chr21:17999000..17999072hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048967
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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