A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379068



Internal ID22436938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46229388..46229656hg38UCSC Ensembl
chr18:43809354..43809622hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937825
Supporting Variants
Samples
Known GenesC18orf25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379068
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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