A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860241



Internal ID22635176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104774997..104777022hg38UCSC Ensembl
chr12:105168775..105170800hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382026
hg192026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860241
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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