A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927936



Internal ID22703169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105742107..105773688hg38UCSC Ensembl
chr14:106208444..106240025hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3831582
hg1931582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv654n209
Supporting Variantsnssv17375772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927936
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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