A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537882



Internal ID20911211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17932269..17985839hg38UCSC Ensembl
chr22:18415035..18468605hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3853571
hg1953571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204521
Samples
Known GenesMICAL3, MIR648
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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