A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851461



Internal ID22626396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114971075..114979064hg38UCSC Ensembl
chr12:115408880..115416869hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg387990
hg197990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851461
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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