A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736109



Internal ID159775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3368587..3369044hg38UCSC Ensembl
chrX:3286628..3287085hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736109
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.015454


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