A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702896



Internal ID126562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64118994..64118994hg38UCSC Ensembl
chr15:64411193..64411193hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414096
Supporting Variants
Samples
Known GenesSNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702896
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.032671


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