A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060184



Internal ID21969417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47732297..47732355hg38UCSC Ensembl
chr22:48128046..48128104hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060184
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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