A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737308



Internal ID160974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119188101..119202449hg38UCSC Ensembl
chrX:118322064..118336412hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3814349
hg1914349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737308
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00166563


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