A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836120



Internal ID22611055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23472335..23477169hg38UCSC Ensembl
chr3:23513826..23518660hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384835
hg194835
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490526
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836120
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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