A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184187



Internal ID20751227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74031715..74542941hg38UCSC Ensembl
chr16:74065614..74576839hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38511227
hg19511226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497036
Supporting Variants
Samples
Known GenesCLEC18B, GLG1, LOC101928035, LOC283922, PSMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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