A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546905



Internal ID20920116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48326670..48339174hg38UCSC Ensembl
chr22:48722482..48734986hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3812505
hg1912505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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