A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741708



Internal ID165374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101098974..101098974hg38UCSC Ensembl
chrX:100353963..100353963hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741708
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00175088


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