A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741971



Internal ID165637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110851224..110852126hg38UCSC Ensembl
chrX:110094452..110095354hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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