A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024607



Internal ID21933950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39583209..39599586hg38UCSC Ensembl
chr14:40052413..40068790hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3816378
hg1916378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024607
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