A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942392



Internal ID22717829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9686857..9689023hg38UCSC Ensembl
chr18:9686854..9689020hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg382167
hg192167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942392
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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