A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937346



Internal ID22712712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35370257..35370706hg38UCSC Ensembl
chr18:32950221..32950670hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389351
Samples
Known GenesZNF396
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937346
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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