A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370878



Internal ID21028431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8815701..8818900hg38UCSC Ensembl
chr3:8857387..8860586hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370878
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