A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373615



Internal ID21031168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9425061..9426272hg38UCSC Ensembl
chr3:9466745..9467956hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210794
Samples
Known GenesSETD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373615
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