A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548228



Internal ID20921424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38642652..38644804hg38UCSC Ensembl
chr22:39038657..39040809hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382153
hg192153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204653
Samples
Known GenesFAM227A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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