A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438354



Internal ID22104533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24323390..24324621hg38UCSC Ensembl
chr18:21903354..21904585hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766049
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438354
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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