A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204623



Internal ID20771663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36725786..36733994hg38UCSC Ensembl
chr22:37121831..37130039hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg388209
hg198209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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