A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646647



Internal ID21838694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27000794..27000794hg38UCSC Ensembl
chr22:27396757..27396757hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646647
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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