A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866777



Internal ID22641712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54265948..54267147hg38UCSC Ensembl
chr12:54659732..54660931hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467694
Samples
Known GenesCBX5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866777
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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