A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538682



Internal ID20911996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48994038..49609170hg38UCSC Ensembl
chr22:49389850..50002818hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38615133
hg19612969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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