A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933360



Internal ID22708671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2830223..2835432hg38UCSC Ensembl
chr18:2830221..2835430hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg385210
hg195210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933360
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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