A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089386



Internal ID21998619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102251639..102251639hg38UCSC Ensembl
chr14:102717976..102717976hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606220
Samples
Known GenesMOK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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