A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050954



Internal ID21960188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21065054..21065916hg38UCSC Ensembl
chr20:21045695..21046557hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050954
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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