A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934376



Internal ID22709701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12433056..12433116hg38UCSC Ensembl
chr18:12433055..12433115hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934376
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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