A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371470



Internal ID21029023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66093580..66188201hg38UCSC Ensembl
chr3:66079255..66170269hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3894622
hg1991015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212985
Samples
Known GenesSLC25A26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371470
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