A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703306



Internal ID126972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94898256..94898307hg38UCSC Ensembl
chr15:95441485..95441536hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426294
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703306
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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