A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639917



Internal ID21831964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42740664..42740664hg38UCSC Ensembl
chr22:43136670..43136670hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639917
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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