A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835866



Internal ID22610801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25485558..25487457hg38UCSC Ensembl
chr3:25527049..25528948hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490576
Samples
Known GenesRARB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835866
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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