A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852097



Internal ID22627032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28431121..28447434hg38UCSC Ensembl
chr14:28900327..28916640hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3816314
hg1916314
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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