A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874679



Internal ID22649632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48860338..48862171hg38UCSC Ensembl
chr19:49363595..49365428hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381834
hg191834
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477327
Samples
Known GenesPLEKHA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874679
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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