A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945774



Internal ID22721255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30379220..30379273hg38UCSC Ensembl
chr14:30848426..30848479hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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