A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206795



Internal ID20773836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40161654..40176324hg38UCSC Ensembl
chr22:40557658..40572328hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3814671
hg1914671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553783
Supporting Variants
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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