A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975355



Internal ID22750290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89670041..89670041hg38UCSC Ensembl
chr14:90136385..90136385hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975355
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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