A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739716



Internal ID163382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23997816..24001564hg38UCSC Ensembl
chrX:24015933..24019681hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg383749
hg193749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427755
Supporting Variants
Samples
Known GenesKLHL15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739716
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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