A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206794



Internal ID20773835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39982414..39987797hg38UCSC Ensembl
chr22:40378418..40383801hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385384
hg195384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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