A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858033



Internal ID22632968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106812710..106816209hg38UCSC Ensembl
chr12:107206488..107209987hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469049
Samples
Known GenesRIC8B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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