A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644612



Internal ID21836659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37837979..37838163hg38UCSC Ensembl
chr22:38233986..38234170hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058590
Supporting Variants
Samples
Known GenesANKRD54
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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