A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741276



Internal ID164942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87663439..87663490hg38UCSC Ensembl
chrX:86918439..86918490hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557239
Supporting Variants
Samples
Known GenesKLHL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741276
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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