A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552227



Internal ID20925355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44674554..44675160hg38UCSC Ensembl
chr22:45070434..45071040hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207552
Samples
Known GenesPRR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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