A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722108



Internal ID145774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19576414..19585600hg38UCSC Ensembl
chr19:19687223..19696409hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg389187
hg199187
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554738
Supporting Variants
Samples
Known GenesPBX4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722108
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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