A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459513



Internal ID22517397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28229856..28303258hg38UCSC Ensembl
chrX:28247973..28321375hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3873403
hg1973403
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459513
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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