A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366280



Internal ID21023833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3323362..3333177hg38UCSC Ensembl
chr4:3325089..3334904hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg389816
hg199816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115652
Samples
Known GenesRGS12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366280
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