A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894689



Internal ID22669764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108530325..108538493hg38UCSC Ensembl
chr4:109451481..109459649hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg388169
hg198169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416180
Samples
Known GenesRPL34-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894689
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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