A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935211



Internal ID22710549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49880266..49891913hg38UCSC Ensembl
chr14:50346984..50358631hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3811648
hg1911648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935211
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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