A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851989



Internal ID22626924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3592314..3613335hg38UCSC Ensembl
chr12:3701480..3722501hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3821022
hg1921022
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465124
Samples
Known GenesPRMT8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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