A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204898



Internal ID20771938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25291333..25588009hg38UCSC Ensembl
chr22:25687300..25983976hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38296677
hg19296677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554574
Supporting Variants
Samples
Known GenesADRBK2, CRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00194


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