A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400198



Internal ID22458068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75657641..75750294hg38UCSC Ensembl
chr18:73369596..73462249hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3892654
hg1992654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400198
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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