A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741896



Internal ID165562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108768542..108775000hg38UCSC Ensembl
chrX:108011772..108018230hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg386459
hg196459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00295047


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