A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866548



Internal ID22641483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92949798..92955585hg38UCSC Ensembl
chr12:93343574..93349361hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg385788
hg195788
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866548
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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