A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862449



Internal ID22637384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73616559..73619079hg38UCSC Ensembl
chr14:74083263..74085783hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382521
hg192521
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465588
Samples
Known GenesACOT6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862449
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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