A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937314



Internal ID22712679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20828565..20828632hg38UCSC Ensembl
chr14:21296724..21296791hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937314
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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