A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740884



Internal ID164550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77758159..77774406hg38UCSC Ensembl
chrX:77013640..77029888hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3816248
hg1916249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420690
Supporting Variants
Samples
Known GenesATRX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00187305


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