A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021109



Internal ID21930452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56503874..56503944hg38UCSC Ensembl
chr14:56970592..56970662hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021109
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