A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736795



Internal ID160461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47469725..47476222hg38UCSC Ensembl
chrX:47329124..47335621hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg386498
hg196498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430074
Supporting Variants
Samples
Known GenesZNF41
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736795
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00208117


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