A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027086



Internal ID21936429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68868439..68868558hg38UCSC Ensembl
chr14:69335156..69335275hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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