A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186456



Internal ID20753496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14646753..14659807hg38UCSC Ensembl
chr16:14740610..14753664hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3813055
hg1913055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502660
Supporting Variants
Samples
Known GenesBFAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186456
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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