A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851796



Internal ID22626731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106810139..106811360hg38UCSC Ensembl
chr12:107203917..107205138hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462896, nssv17461333
Samples
Known GenesRIC8B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851796
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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