A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863126



Internal ID22638061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116657274..116661131hg38UCSC Ensembl
chr12:117095079..117098936hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863126
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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