A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834368



Internal ID22609303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151759845..151762227hg38UCSC Ensembl
chr3:151477633..151480015hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485697
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834368
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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