A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185732



Internal ID20752772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68196373..68218824hg38UCSC Ensembl
chr16:68230276..68252727hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3822452
hg1922452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507364
Supporting Variants
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185732
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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