A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939049



Internal ID22714437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10464317..10465438hg38UCSC Ensembl
chr19:10574993..10576114hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408359
Samples
Known GenesPDE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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