A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547408



Internal ID20920609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40195201..40203700hg38UCSC Ensembl
chr22:40591205..40599704hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073813
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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