A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406829



Internal ID22464699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75108277..75108277hg38UCSC Ensembl
chr18:72820233..72820233hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980058
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406829
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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