A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741904



Internal ID165570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108894244..108907058hg38UCSC Ensembl
chrX:108137474..108150288hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3812815
hg1912815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424025
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741904
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00104058


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