A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190393



Internal ID20757434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:73789935..74447058hg38UCSC Ensembl
chr16:73823834..74480956hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38657124
hg19657123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503615
Supporting Variants
Samples
Known GenesCLEC18B, LOC101928035, LOC283922, PSMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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