A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046187



Internal ID21955432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38160604..38165631hg38UCSC Ensembl
chr22:38556611..38561638hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385028
hg195028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638092
Samples
Known GenesPLA2G6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046187
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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