A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738604



Internal ID162270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:811369..821714hg38UCSC Ensembl
chrX:772104..782449hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3810346
hg1910346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738604
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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