A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735314



Internal ID158980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8515867..8515918hg38UCSC Ensembl
chr5:8515979..8516030hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735314
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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