A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514610



Internal ID20887965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103884018..103884393hg38UCSC Ensembl
chr14:104350355..104350730hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514610
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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