A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739769



Internal ID163435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25286787..25286790hg38UCSC Ensembl
chrX:25304904..25304907hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739769
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003746


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