A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535711



Internal ID20909065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26503252..26503616hg38UCSC Ensembl
chr22:26899218..26899582hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204950
Samples
Known GenesTFIP11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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