A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329859



Internal ID20863012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20836858..20839108hg38UCSC Ensembl
chr1:21163351..21165601hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382251
hg192251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057186
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329859
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