A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204663



Internal ID20771703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38983345..39022186hg38UCSC Ensembl
chr22:39379350..39418191hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3838842
hg1938842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540696
Supporting Variants
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1, APOBEC3C, APOBEC3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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