A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836829



Internal ID22611764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79615847..79622546hg38UCSC Ensembl
chr3:79664997..79671696hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495454
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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