A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742074



Internal ID165740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113862000..113868542hg38UCSC Ensembl
chrX:113105283..113111825hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg386543
hg196543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742074
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000837346


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