A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848821



Internal ID22623756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29902120..29932556hg38UCSC Ensembl
chr14:30371326..30401762hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3830437
hg1930437
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469211
Samples
Known GenesPRKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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