A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742356



Internal ID166022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132035594..132037642hg38UCSC Ensembl
chrX:131169622..131171670hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg382049
hg192049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422335
Supporting Variants
Samples
Known GenesMST4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742356
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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