A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933604



Internal ID22708918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18163785..18164088hg38UCSC Ensembl
chr19:18274595..18274898hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390944
Samples
Known GenesPIK3R2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933604
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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