A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051930



Internal ID21961163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41564475..41564553hg38UCSC Ensembl
chr22:41960479..41960557hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640446
Samples
Known GenesCSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051930
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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