A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866646



Internal ID22641581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23795608..23802839hg38UCSC Ensembl
chr14:24264817..24272048hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387232
hg197232
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866646
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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