A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646031



Internal ID21838078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36126363..36126953hg38UCSC Ensembl
chr22:36522411..36523001hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646031
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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