A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855462



Internal ID22630397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25171571..25185423hg38UCSC Ensembl
chr14:25640777..25654629hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3813853
hg1913853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855462
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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