A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861090



Internal ID22636025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55565695..55567578hg38UCSC Ensembl
chr12:55959479..55961362hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468536, nssv17452896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861090
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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