A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736759



Internal ID160425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46739957..46740008hg38UCSC Ensembl
chrX:46599392..46599443hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562282
Supporting Variants
Samples
Known GenesSLC9A7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736759
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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