A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730960



Internal ID20506877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100873198..100873887hg38UCSC Ensembl
chr14:101339535..101340224hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730960
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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