A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857730



Internal ID22632665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21441572..21443602hg38UCSC Ensembl
chr14:21909731..21911761hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382031
hg192031
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857730
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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