A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038399



Internal ID93330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87914770..87914770hg38UCSC Ensembl
chr10:89674527..89674527hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409192
Supporting Variants
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038399
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004374


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