A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193046



Internal ID20760087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56457943..56465265hg38UCSC Ensembl
chr16:56491855..56499177hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387323
hg197323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503237
Supporting Variants
Samples
Known GenesOGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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