A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736263



Internal ID159929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26792900..26803600hg38UCSC Ensembl
chrX:26811017..26821717hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3810701
hg1910701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736263
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00405204


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