A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700144



Internal ID123810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40840626..40840677hg38UCSC Ensembl
chr15:41132824..41132875hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700144
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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