A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644825



Internal ID21836872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35578409..35578409hg38UCSC Ensembl
chr22:35974456..35974456hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644825
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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