A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735948



Internal ID159614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:266351..272351hg38UCSC Ensembl
chrX:183018..189018hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428615
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735948
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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