A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427331



Internal ID206236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115565342..115567043hg38UCSC Ensembl
chrX:114799668..114801365hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381702
hg191698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742139
Samples
Known GenesPLS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427331
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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