A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479289



Internal ID22537191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73715037..73723255hg38UCSC Ensembl
chr18:71382272..71390490hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg388219
hg198219
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479289
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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