A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638730



Internal ID21830777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41939778..41939907hg38UCSC Ensembl
chr22:42335782..42335911hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057167
Supporting Variants
Samples
Known GenesCENPM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638730
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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