A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892550



Internal ID22667603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154136211..154136278hg38UCSC Ensembl
chr3:153854000..153854067hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413709, nssv17419659
Samples
Known GenesARHGEF26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892550
Frequency
Sample Size914
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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