A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547167



Internal ID20920373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20544402..20685926hg38UCSC Ensembl
chr22:20898689..21040214hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38141525
hg19141526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206671
Samples
Known GenesMED15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547167
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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