A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703583



Internal ID127249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84682310..84682361hg38UCSC Ensembl
chr15:85225541..85225592hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422601
Supporting Variants
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703583
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004683


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