A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047273



Internal ID21956506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26797622..26801909hg38UCSC Ensembl
chr21:28169941..28174228hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384288
hg194288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047273
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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