A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939158



Internal ID22714547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29550379..29939053hg38UCSC Ensembl
chr18:27130344..27519018hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38388675
hg19388675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939158
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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