A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741063



Internal ID164729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81893230..81895600hg38UCSC Ensembl
chrX:81148729..81151099hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg382371
hg192371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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