A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638467



Internal ID21830514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38527486..38528346hg38UCSC Ensembl
chr22:38923491..38924351hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042493
Supporting Variants
Samples
Known GenesDMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638467
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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