A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538477



Internal ID20911794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45046168..45059059hg38UCSC Ensembl
chr22:45442049..45454940hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3812892
hg1912892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4728n223
Supporting Variantsnssv18207561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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