A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381288



Internal ID22439158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11218425..11234786hg38UCSC Ensembl
chr18:11218424..11234785hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3816362
hg1916362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381288
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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