A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445465



Internal ID22503335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100724910..100774493hg38UCSC Ensembl
chrX:99979898..100029482hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3849584
hg1949585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880646
Supporting Variants
Samples
Known GenesSYTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445465
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00


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