A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859998



Internal ID22634933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10845386..10851910hg38UCSC Ensembl
chr12:10997985..11004509hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg386525
hg196525
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462718
Samples
Known GenesPRH1-PRR4, PRR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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