A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422831



Internal ID201866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:279568..294063hg38UCSC Ensembl
chrX:196235..210730hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3814496
hg1914496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735958
Samples
Known GenesPLCXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422831
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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