A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879769



Internal ID22654741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48871636..48884125hg38UCSC Ensembl
chr19:49374893..49387382hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3812490
hg1912490
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477328
Samples
Known GenesPPP1R15A, TULP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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