A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453961



Internal ID22511836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11018735..11021842hg38UCSC Ensembl
chr12:11171334..11174441hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg383108
hg193108
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864034
Supporting Variants
Samples
Known GenesPRH1-PRR4, TAS2R19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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