A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864604



Internal ID22639539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49326472..49327671hg38UCSC Ensembl
chr12:49720255..49721454hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464372
Samples
Known GenesTROAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864604
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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