A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941902



Internal ID22717333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72395362..72395502hg38UCSC Ensembl
chr18:70062597..70062737hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941902
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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