A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857659



Internal ID22632594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54485577..54491339hg38UCSC Ensembl
chr12:54879361..54885123hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg385763
hg195763
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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