A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205029



Internal ID20772069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32353734..32409835hg38UCSC Ensembl
chr22:32749721..32805822hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3856102
hg1956102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550876
Supporting Variants
Samples
Known GenesLOC339666, RFPL3, RFPL3S, RTCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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