A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197981



Internal ID20765021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80227796..80262675hg38UCSC Ensembl
chr18:77985679..78017154hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3834880
hg1931476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518932
Supporting Variants
Samples
Known GenesPARD6G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197981
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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