A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735962



Internal ID159628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:292798..304449hg38UCSC Ensembl
chrX:209465..221116hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3811652
hg1911652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427781
Supporting Variants
Samples
Known GenesPLCXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735962
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00104471


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