A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741885



Internal ID165551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108139603..108141098hg38UCSC Ensembl
chrX:107382833..107384328hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426377
Supporting Variants
Samples
Known GenesATG4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741885
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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