A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864051



Internal ID22638986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61363703..61385298hg38UCSC Ensembl
chr14:61830421..61852016hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3821596
hg1921596
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467119
Samples
Known GenesPRKCH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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