A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053856



Internal ID21963089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45890371..45890493hg38UCSC Ensembl
chr21:47310285..47310407hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642794
Samples
Known GenesPCBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053856
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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