A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941005



Internal ID22716422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64577968..64578196hg38UCSC Ensembl
chr14:65044686..65044914hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385529
Samples
Known GenesPPP1R36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941005
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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