A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853365



Internal ID22628300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77812577..77818229hg38UCSC Ensembl
chr14:78278920..78284572hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385653
hg195653
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454331
Samples
Known GenesADCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer