A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555122



Internal ID20928211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38942401..39002700hg38UCSC Ensembl
chr22:39338406..39398705hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3860300
hg1960300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204660
Samples
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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