A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355861



Internal ID21013414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5190941..5350984hg38UCSC Ensembl
chr3:5232626..5392669hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38160044
hg19160044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100950
Samples
Known GenesEDEM1, MIR4790
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355861
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