A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514646



Internal ID20888001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69385001..69386900hg38UCSC Ensembl
chr16:69418904..69420803hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180129
Samples
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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