A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859567



Internal ID22634502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73487581..73495263hg38UCSC Ensembl
chr14:73954286..73961967hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387683
hg197682
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451033
Samples
Known GenesC14orf169, HEATR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859567
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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