A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737823



Internal ID161489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147231729..147231837hg38UCSC Ensembl
chrX:146313247..146313355hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737823
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.150501


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