A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057097



Internal ID21966330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32583792..32583862hg38UCSC Ensembl
chr22:32979778..32979848hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640237
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057097
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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