A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851316



Internal ID22626251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54141877..54144176hg38UCSC Ensembl
chr12:54535661..54537960hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851316
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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