A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17718360



Internal ID142026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54923272..54923323hg38UCSC Ensembl
chr18:52590503..52590554hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421683
Supporting Variants
Samples
Known GenesCCDC68
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17718360
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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