A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046670



Internal ID21955903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25606200..25606309hg38UCSC Ensembl
chr21:26978512..26978621hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637948
Samples
Known GenesMRPL39
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046670
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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