A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840084



Internal ID22615019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68809771..68822524hg38UCSC Ensembl
chr4:69675489..69688242hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3812754
hg1912754
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1578n209
Supporting Variantsnssv17497144, nssv17497145
Samples
Known GenesUGT2B10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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