A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036611



Internal ID92154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95644320..95644371hg38UCSC Ensembl
chr10:97404077..97404128hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554180
Supporting Variants
Samples
Known GenesALDH18A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036611
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer