A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552439



Internal ID20925567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32944685..32954671hg38UCSC Ensembl
chr22:33340670..33350656hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg389987
hg199987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204570
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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