A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738656



Internal ID162322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:968973..1193208hg38UCSC Ensembl
chrX:929708..1264234hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38224236
hg19334527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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