A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712836



Internal ID136502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35934565..35934616hg38UCSC Ensembl
chr17:34261569..34261620hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425415
Supporting Variants
Samples
Known GenesLYZL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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