A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864869



Internal ID22639804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125809385..125810584hg38UCSC Ensembl
chr12:126293931..126295130hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864869
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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