A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736118



Internal ID159784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3586883..3639484hg38UCSC Ensembl
chrX:3504924..3557525hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3852602
hg1952602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138316
Supporting Variants
Samples
Known GenesPRKX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736118
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00041658


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