A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537374



Internal ID20910712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40225202..40237579hg38UCSC Ensembl
chr22:40621206..40633583hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3812378
hg1912378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073817
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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