A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206822



Internal ID20773863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41549556..41590685hg38UCSC Ensembl
chr22:41945560..41986689hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3841130
hg1941130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550267
Supporting Variants
Samples
Known GenesCSDC2, PMM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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