A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190632



Internal ID20757672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32107901..32139200hg38UCSC Ensembl
chr18:29687864..29719163hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3831300
hg1931300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532981
Supporting Variants
Samples
Known GenesRNF138
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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