A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739967



Internal ID163633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33748072..33748123hg38UCSC Ensembl
chrX:33766189..33766240hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739967
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001561


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