A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738146



Internal ID161812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154739674..154739782hg38UCSC Ensembl
chrX:153967949..153968057hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422370
Supporting Variants
Samples
Known GenesGAB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738146
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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