A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740885



Internal ID164551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77789755..77890002hg38UCSC Ensembl
chrX:77045234..77145499hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38100248
hg19100266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422154
Supporting Variants
Samples
Known GenesMAGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740885
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0012487


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