A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851143



Internal ID22626078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98916728..98918427hg38UCSC Ensembl
chr14:99383065..99384764hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv616n209
Supporting Variantsnssv17470239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851143
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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