A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700141



Internal ID123807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40808120..40808120hg38UCSC Ensembl
chr15:41100318..41100318hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426942
Supporting Variants
Samples
Known GenesZFYVE19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700141
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.337295


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