A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864034



Internal ID22638969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11018735..11021842hg38UCSC Ensembl
chr12:11171334..11174441hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg383108
hg193108
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464756, nssv17453961
Samples
Known GenesPRH1-PRR4, TAS2R19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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