A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370865



Internal ID21028418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79612876..79691096hg38UCSC Ensembl
chr3:79662026..79740246hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3878221
hg1978221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104604
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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