A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880055



Internal ID22655025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41283631..41287830hg38UCSC Ensembl
chr19:41789536..41793735hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475955
Samples
Known GenesHNRNPUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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