A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935485



Internal ID22710828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105746515..105773737hg38UCSC Ensembl
chr14:106212852..106240074hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3827223
hg1927223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv654n209
Supporting Variantsnssv17377801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935485
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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