A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553557



Internal ID20926667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32782333..32786627hg38UCSC Ensembl
chr22:33178319..33182613hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384295
hg194295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204568
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553557
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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