A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355990



Internal ID21013543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49313247..49318003hg38UCSC Ensembl
chr3:49350680..49355436hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384757
hg194757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102039
Samples
Known GenesUSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355990
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