A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553061



Internal ID20926176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38648358..38655378hg38UCSC Ensembl
chr22:39044363..39051383hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387021
hg197021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204654
Samples
Known GenesFAM227A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553061
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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