A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851951



Internal ID22626886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65155446..65163376hg38UCSC Ensembl
chr14:65622164..65630094hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg387931
hg197931
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851951
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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