A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835286



Internal ID22610221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154028529..154030094hg38UCSC Ensembl
chr3:153746318..153747883hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485737
Samples
Known GenesARHGEF26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835286
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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