A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643754



Internal ID21835801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45031813..45031813hg38UCSC Ensembl
chr22:45427694..45427694hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643754
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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