A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742153



Internal ID165819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115939244..115969853hg38UCSC Ensembl
chrX:115055577..115086186hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3830610
hg1930610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000832466


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