A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884372



Internal ID22659354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55203329..55206364hg38UCSC Ensembl
chr19:55714697..55717732hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383036
hg193036
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478725, nssv17478724
Samples
Known GenesPTPRH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884372
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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