A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052927



Internal ID21962160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35438185..35438713hg38UCSC Ensembl
chr22:35834178..35834706hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052927
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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