A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937062



Internal ID22712425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105746069..105773374hg38UCSC Ensembl
chr14:106212406..106239711hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3827306
hg1927306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv654n209
Supporting Variantsnssv17387014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937062
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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