A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892001



Internal ID22667045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20054861..20362981hg38UCSC Ensembl
chr3:20096353..20404473hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38308121
hg19308121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424048
Samples
Known GenesKAT2B, SGOL1, SGOL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892001
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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