A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888393



Internal ID22663398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35977015..35977074hg38UCSC Ensembl
chr5:35977117..35977176hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426898
Samples
Known GenesUGT3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888393
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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